Canonical Allele Identifier: CA1565569289

Gene: CAST ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96762325A= , CM000667.2:g.96762325A=	GRCh38
NC_000005.9:g.96098029A= , CM000667.1:g.96098029A=	GRCh37
NC_000005.8:g.96123785A=	NCBI36
NG_027839.1:g.56820T=
NG_029490.1:g.105289A=
NG_027839.2:g.178659T=
NG_029490.2:g.105289A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484552.6:c.805A= (CAST)	ENSP00000432878.2:p.Thr269=
ENST00000508608.6:c.1735A= (CAST)	ENSP00000422677.2:p.Thr579=
ENST00000510756.6:c.1513A= (CAST)	ENSP00000422176.2:p.Thr505=
ENST00000674587.1:c.1342A= (CAST)	ENSP00000501797.1:p.Thr448=
ENST00000674702.1:c.1627A= (CAST)	ENSP00000502345.1:p.Thr543=
ENST00000674984.1:c.1819A= (CAST)	ENSP00000501713.1:p.Thr607=
ENST00000675033.1:c.1513A= (CAST)	ENSP00000501659.1:p.Thr505=
ENST00000675179.1:c.1885A= (CAST) MANE Select	ENSP00000501872.1:p.Thr629=
ENST00000675185.1:c.266A= (CAST)
ENST00000675266.1:c.1787A= (CAST)
ENST00000675267.1:c.*1509A= (CAST)	ENSP00000502095.1:n.*1509A=
ENST00000675275.1:c.602A= (CAST)
ENST00000675479.1:c.1498A= (CAST)	ENSP00000502244.1:p.Thr500=
ENST00000675614.1:c.1555A= (CAST)	ENSP00000502136.1:p.Thr519=
ENST00000675663.1:c.1774A= (CAST)	ENSP00000502449.1:p.Thr592=
ENST00000675734.1:n.429A= (CAST)
ENST00000675858.1:c.1429A= (CAST)	ENSP00000501780.1:p.Thr477=
ENST00000296754.7:c.*875T= (ERAP1)	ENSP00000296754.3:n.*875T=
ENST00000309190.9:c.1570A= (CAST)	ENSP00000312523.5:p.Thr524=
ENST00000325674.11:c.805A= (CAST)	ENSP00000320319.8:p.Thr269=
ENST00000338252.7:c.1597A= (CAST)	ENSP00000343421.3:p.Thr533=
ENST00000341926.7:c.1636A= (CAST)	ENSP00000339914.3:p.Thr546=
ENST00000348386.7:n.1578A= (CAST)
ENST00000395812.6:c.1762A= (CAST)	ENSP00000379157.2:p.Thr588=
ENST00000395813.5:c.1636A= (CAST)	ENSP00000379158.2:p.Thr546=
ENST00000437034.6:c.891A= (CAST)
ENST00000484552.5:c.863A= (CAST)
ENST00000504465.5:c.1420A= (CAST)	ENSP00000425670.1:p.Thr474=
ENST00000508579.5:c.781A= (CAST)	ENSP00000425787.1:p.Thr261=
ENST00000508608.5:c.1774A= (CAST)	ENSP00000422677.1:p.Thr592=
ENST00000508830.5:c.1885A= (CAST)	ENSP00000425721.1:p.Thr629=
ENST00000509903.5:c.1531A= (CAST)	ENSP00000426946.1:p.Thr511=
ENST00000510098.1:c.121A= (CAST)	ENSP00000427195.1:p.Thr41=
ENST00000510156.5:c.1636A= (CAST)	ENSP00000422325.1:p.Thr546=
ENST00000510500.5:c.908A= (CAST)
ENST00000510756.5:c.1819A= (CAST)	ENSP00000422176.1:p.Thr607=
ENST00000511049.5:c.1594A= (CAST)	ENSP00000421130.1:p.Thr532=
ENST00000511782.5:c.1594A= (CAST)	ENSP00000423638.1:p.Thr532=
ENST00000515663.5:c.805A= (CAST)	ENSP00000422929.1:p.Thr269=
NM_001042440.3:c.1762A= (CAST)	NP_001035905.1:p.Thr588=
NM_001190442.1:c.1597A= (CAST)	NP_001177371.1:p.Thr533=
NM_001284212.1:c.1513A= (CAST)	NP_001271141.1:p.Thr505=
NM_001284213.1:c.1420A= (CAST)	NP_001271142.1:p.Thr474=
NM_016442.3:c.*875T= (ERAP1)	NP_057526.3:n.*875T=
NM_173060.3:c.1570A= (CAST)	NP_775083.1:p.Thr524=
NR_104285.1:n.892A= (CAST)
XM_006714696.2:c.1885A= (CAST)	XP_006714759.1:p.Thr629=
XM_006714697.2:c.1885A= (CAST)	XP_006714760.1:p.Thr629=
XM_006714698.2:c.1846A= (CAST)	XP_006714761.1:p.Thr616=
XM_006714699.2:c.1840A= (CAST)	XP_006714762.1:p.Thr614=
XM_006714700.2:c.1828A= (CAST)	XP_006714763.1:p.Thr610=
XM_006714701.2:c.1819A= (CAST)	XP_006714764.1:p.Thr607=
XM_006714702.2:c.1783A= (CAST)	XP_006714765.1:p.Thr595=
XM_006714703.2:c.1780A= (CAST)	XP_006714766.1:p.Thr594=
XM_006714704.2:c.1774A= (CAST)	XP_006714767.1:p.Thr592=
XM_006714705.2:c.1762A= (CAST)	XP_006714768.1:p.Thr588=
XM_006714706.2:c.1717A= (CAST)	XP_006714769.1:p.Thr573=
XM_006714707.2:c.1636A= (CAST)	XP_006714770.1:p.Thr546=
XM_006714708.2:c.1597A= (CAST)	XP_006714771.1:p.Thr533=
XM_006714709.2:c.1579A= (CAST)	XP_006714772.1:p.Thr527=
XM_006714710.2:c.1531A= (CAST)	XP_006714773.1:p.Thr511=
XM_006714711.2:c.1513A= (CAST)	XP_006714774.1:p.Thr505=
XM_006714712.2:c.1474A= (CAST)	XP_006714775.1:p.Thr492=
XM_006714713.2:c.805A= (CAST)	XP_006714776.1:p.Thr269=
XM_006714714.2:c.805A= (CAST)	XP_006714777.1:p.Thr269=
XM_006714715.2:c.781A= (CAST)	XP_006714778.1:p.Thr261=
XM_011543487.1:c.*875T= (ERAP1)	XP_011541789.1:n.*875T=
XM_011543654.1:c.1804A= (CAST)	XP_011541956.1:p.Thr602=
XM_011543655.1:c.1801A= (CAST)	XP_011541957.1:p.Thr601=
XM_011543656.1:c.1738A= (CAST)	XP_011541958.1:p.Thr580=
XM_011543657.1:c.1693A= (CAST)	XP_011541959.1:p.Thr565=
XM_011543658.1:c.1489A= (CAST)	XP_011541960.1:p.Thr497=
NM_001042440.4:c.1762A= (CAST)	NP_001035905.1:p.Thr588=
NM_001042441.2:c.1828A= (CAST)	NP_001035906.1:p.Thr610=
NM_001042442.2:c.1819A= (CAST)	NP_001035907.1:p.Thr607=
NM_001042443.2:c.1636A= (CAST)	NP_001035908.1:p.Thr546=
NM_001042444.2:c.1513A= (CAST)	NP_001035909.1:p.Thr505=
NM_001042445.2:c.1531A= (CAST)	NP_001035910.1:p.Thr511=
NM_001042446.2:c.1474A= (CAST)	NP_001035911.1:p.Thr492=
NM_001284212.3:c.1513A= (CAST)	NP_001271141.1:p.Thr505=
NM_001284213.3:c.1420A= (CAST)	NP_001271142.1:p.Thr474=
NM_001330626.1:c.1789A= (CAST)	NP_001317555.1:p.Thr597=
NM_001330627.1:c.1762A= (CAST)	NP_001317556.1:p.Thr588=
NM_001330628.1:c.1717A= (CAST)	NP_001317557.1:p.Thr573=
NM_001330629.1:c.1801A= (CAST)	NP_001317558.1:p.Thr601=
NM_001330630.1:c.1474A= (CAST)	NP_001317559.1:p.Thr492=
NM_001330631.1:c.1597A= (CAST)	NP_001317560.1:p.Thr533=
NM_001330632.1:c.1570A= (CAST)	NP_001317561.1:p.Thr524=
NM_001330633.1:c.1579A= (CAST)	NP_001317562.1:p.Thr527=
NM_001330634.1:c.1540A= (CAST)	NP_001317563.1:p.Thr514=
NM_001349244.1:c.*875T= (ERAP1)	NP_001336173.1:n.*875T=
NM_001750.6:c.1885A= (CAST)	NP_001741.4:p.Thr629=
NM_016442.4:c.*875T= (ERAP1)	NP_057526.3:n.*875T=
NM_173060.4:c.1570A= (CAST)	NP_775083.1:p.Thr524=
XR_001742119.2:n.3860T= (ERAP1)
NM_001042440.5:c.1762A= (CAST)	NP_001035905.1:p.Thr588=
NM_001042441.3:c.1828A= (CAST)	NP_001035906.1:p.Thr610=
NM_001042442.3:c.1819A= (CAST)	NP_001035907.1:p.Thr607=
NM_001330626.2:c.1789A= (CAST)	NP_001317555.1:p.Thr597=
NM_001330627.2:c.1762A= (CAST)	NP_001317556.1:p.Thr588=
NM_001330628.2:c.1717A= (CAST)	NP_001317557.1:p.Thr573=
NM_001330629.2:c.1801A= (CAST)	NP_001317558.1:p.Thr601=
NM_001375317.1:c.1774A= (CAST)	NP_001362246.1:p.Thr592=
NM_001750.7:c.1885A= (CAST) MANE Select	NP_001741.4:p.Thr629=
NR_104285.2:n.830A= (CAST)
NM_001042443.3:c.1636A= (CAST)	NP_001035908.1:p.Thr546=
NM_001042444.3:c.1513A= (CAST)	NP_001035909.1:p.Thr505=
NM_001042445.3:c.1531A= (CAST)	NP_001035910.1:p.Thr511=
NM_001042446.3:c.1474A= (CAST)	NP_001035911.1:p.Thr492=
NM_001190442.2:c.1597A= (CAST)	NP_001177371.1:p.Thr533=
NM_001284212.4:c.1513A= (CAST)	NP_001271141.1:p.Thr505=
NM_001284213.4:c.1420A= (CAST)	NP_001271142.1:p.Thr474=
NM_001330630.2:c.1474A= (CAST)	NP_001317559.1:p.Thr492=
NM_001330631.2:c.1597A= (CAST)	NP_001317560.1:p.Thr533=
NM_001330632.2:c.1570A= (CAST)	NP_001317561.1:p.Thr524=
NM_001330633.2:c.1579A= (CAST)	NP_001317562.1:p.Thr527=
NM_001330634.2:c.1540A= (CAST)	NP_001317563.1:p.Thr514=
NM_001349244.2:c.*875T= (ERAP1)	NP_001336173.1:n.*875T=
NM_016442.5:c.*875T= (ERAP1)	NP_057526.3:n.*875T=
NM_173060.5:c.1570A= (CAST)	NP_775083.1:p.Thr524=