Canonical Allele Identifier: CA1565576879

Gene: ERAP1 CAST

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96777169A= , CM000667.2:g.96777169A=	GRCh38
NC_000005.9:g.96112873A= , CM000667.1:g.96112873A=	GRCh37
NC_000005.8:g.96138629A=	NCBI36
NG_027839.1:g.41976T=
NG_027839.2:g.163815T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.2671-618T= (ERAP1) MANE Select	ENSP00000406304.2:n.2671-618T=
ENST00000296754.7:c.2671-618T= (ERAP1)	ENSP00000296754.3:n.2671-618T=
ENST00000443439.6:c.2671-618T= (ERAP1)	ENSP00000406304.2:n.2671-618T=
ENST00000510098.1:c.1049+215A= (CAST)	ENSP00000427195.1:n.1049+215A=
ENST00000512852.1:c.207-618T= (ERAP1)
NM_001040458.1:c.2671-618T= (ERAP1)	NP_001035548.1:n.2671-618T=
NM_001198541.1:c.2671-618T= (ERAP1)	NP_001185470.1:n.2671-618T=
NM_016442.3:c.2671-618T= (ERAP1)	NP_057526.3:n.2671-618T=
XM_005272015.3:c.2671-618T= (ERAP1)	XP_005272072.1:n.2671-618T=
XM_005272016.3:c.2671-618T= (ERAP1)	XP_005272073.1:n.2671-618T=
XM_011543480.1:c.2671-618T= (ERAP1)	XP_011541782.1:n.2671-618T=
XM_011543481.1:c.2671-618T= (ERAP1)	XP_011541783.1:n.2671-618T=
XM_011543482.1:c.2671-618T= (ERAP1)	XP_011541784.1:n.2671-618T=
XM_011543483.1:c.2671-618T= (ERAP1)	XP_011541785.1:n.2671-618T=
XM_011543484.1:c.2671-618T= (ERAP1)	XP_011541786.1:n.2671-618T=
XM_011543485.1:c.2671-618T= (ERAP1)	XP_011541787.1:n.2671-618T=
XM_011543486.1:c.2671-618T= (ERAP1)	XP_011541788.1:n.2671-618T=
XM_011543487.1:c.2671-618T= (ERAP1)	XP_011541789.1:n.2671-618T=
XR_948593.1:n.397+215A=
XR_948595.1:n.397+215A=
NM_001040458.2:c.2671-618T= (ERAP1)	NP_001035548.1:n.2671-618T=
NM_001198541.2:c.2671-618T= (ERAP1)	NP_001185470.1:n.2671-618T=
NM_001349244.1:c.2671-618T= (ERAP1)	NP_001336173.1:n.2671-618T=
NM_016442.4:c.2671-618T= (ERAP1)	NP_057526.3:n.2671-618T=
XM_005272015.5:c.2671-618T= (ERAP1)	XP_005272072.1:n.2671-618T=
XM_005272016.4:c.2671-618T= (ERAP1)	XP_005272073.1:n.2671-618T=
XM_011543480.2:c.2671-618T= (ERAP1)	XP_011541782.1:n.2671-618T=
XM_011543481.2:c.2671-618T= (ERAP1)	XP_011541783.1:n.2671-618T=
XM_011543484.2:c.2671-618T= (ERAP1)	XP_011541786.1:n.2671-618T=
XM_011543485.2:c.2671-618T= (ERAP1)	XP_011541787.1:n.2671-618T=
XM_011543486.3:c.2671-618T= (ERAP1)	XP_011541788.1:n.2671-618T=
XM_017009581.1:c.2671-618T= (ERAP1)	XP_016865070.1:n.2671-618T=
XM_017009583.2:c.1576-618T= (ERAP1)	XP_016865072.1:n.1576-618T=
XM_024446113.1:c.2671-618T= (ERAP1)	XP_024301881.1:n.2671-618T=
XR_001742119.2:n.2809-618T= (ERAP1)
XR_001742445.1:n.408+215A=
XR_001742446.1:n.408+215A=
NM_001040458.3:c.2671-618T= (ERAP1) MANE Select	NP_001035548.1:n.2671-618T=
NM_001198541.3:c.2671-618T= (ERAP1)	NP_001185470.1:n.2671-618T=
NM_001349244.2:c.2671-618T= (ERAP1)	NP_001336173.1:n.2671-618T=
NM_016442.5:c.2671-618T= (ERAP1)	NP_057526.3:n.2671-618T=