Canonical Allele Identifier: CA359474286

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154051A>T (hg19) ; chr5:g.37153949A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153949A>T , CM000667.2:g.37153949A>T	GRCh38
NC_000005.9:g.37154051A>T , CM000667.1:g.37154051A>T	GRCh37
NC_000005.8:g.37189808A>T	NCBI36
NG_032772.1:g.100480T>A
NG_032772.2:g.100480T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1163T>A
ENST00000651892.2:c.8164T>A MANE Select	ENSP00000498265.2:p.Ser2722Thr
ENST00000425232.6:c.8002T>A	ENSP00000389014.2:p.Ser2668Thr
ENST00000508244.5:c.8002T>A	ENSP00000421690.1:p.Ser2668Thr
ENST00000509849.5:c.5176T>A	ENSP00000426337.1:p.Ser1726Thr
ENST00000509957.5:n.406T>A
ENST00000511210.5:n.455T>A
ENST00000511824.2:c.1278T>A
ENST00000514429.5:c.5200T>A	ENSP00000424223.1:p.Ser1734Thr
ENST00000515380.1:n.416T>A
NM_023073.3:c.8002T>A	NP_075561.3:p.Ser2668Thr
XM_005248345.2:c.8164T>A	XP_005248402.1:p.Ser2722Thr
XM_005248346.2:c.8161T>A	XP_005248403.1:p.Ser2721Thr
XM_005248347.2:c.8161T>A	XP_005248404.1:p.Ser2721Thr
XM_005248349.2:c.8053T>A	XP_005248406.1:p.Ser2685Thr
XM_005248350.2:c.8035T>A	XP_005248407.1:p.Ser2679Thr
XM_005248353.3:c.4807T>A	XP_005248410.1:p.Ser1603Thr
XM_006714489.2:c.8164T>A	XP_006714552.1:p.Ser2722Thr
XM_006714491.2:c.2737T>A	XP_006714554.1:p.Ser913Thr
XM_011514085.1:c.8164T>A	XP_011512387.1:p.Ser2722Thr
XM_011514086.1:c.8164T>A	XP_011512388.1:p.Ser2722Thr
XM_011514087.1:c.8110T>A	XP_011512389.1:p.Ser2704Thr
XM_011514088.1:c.8056T>A	XP_011512390.1:p.Ser2686Thr
XM_011514089.1:c.8164T>A	XP_011512391.1:p.Ser2722Thr
XM_011514090.1:c.7846T>A	XP_011512392.1:p.Ser2616Thr
XM_011514091.1:c.7492T>A	XP_011512393.1:p.Ser2498Thr
XM_011514092.1:c.8164T>A	XP_011512394.1:p.Ser2722Thr
XM_011514094.1:c.5389T>A	XP_011512396.1:p.Ser1797Thr
XR_427661.2:n.8339T>A
XR_925644.1:n.8339T>A
XM_005248345.4:c.8164T>A	XP_005248402.1:p.Ser2722Thr
XM_005248346.4:c.8161T>A	XP_005248403.1:p.Ser2721Thr
XM_005248347.4:c.8161T>A	XP_005248404.1:p.Ser2721Thr
XM_005248349.4:c.8053T>A	XP_005248406.1:p.Ser2685Thr
XM_005248350.4:c.8035T>A	XP_005248407.1:p.Ser2679Thr
XM_006714491.3:c.2737T>A	XP_006714554.1:p.Ser913Thr
XM_011514085.3:c.8164T>A	XP_011512387.1:p.Ser2722Thr
XM_011514086.3:c.8164T>A	XP_011512388.1:p.Ser2722Thr
XM_011514087.2:c.8110T>A	XP_011512389.1:p.Ser2704Thr
XM_011514088.2:c.8056T>A	XP_011512390.1:p.Ser2686Thr
XM_011514089.2:c.8164T>A	XP_011512391.1:p.Ser2722Thr
XM_011514090.3:c.7846T>A	XP_011512392.1:p.Ser2616Thr
XM_011514092.2:c.8164T>A	XP_011512394.1:p.Ser2722Thr
XM_011514094.2:c.5389T>A	XP_011512396.1:p.Ser1797Thr
XM_017009760.1:c.7975T>A	XP_016865249.1:p.Ser2659Thr
XM_017009761.2:c.7975T>A	XP_016865250.1:p.Ser2659Thr
XM_017009763.1:c.7171T>A	XP_016865252.1:p.Ser2391Thr
XM_017009765.1:c.6976T>A	XP_016865254.1:p.Ser2326Thr
XM_017009766.1:c.4807T>A	XP_016865255.1:p.Ser1603Thr
XM_024446183.1:c.7975T>A	XP_024301951.1:p.Ser2659Thr
XM_024446184.1:c.7846T>A	XP_024301952.1:p.Ser2616Thr
XM_024446185.1:c.7492T>A	XP_024301953.1:p.Ser2498Thr
XM_024446186.1:c.7171T>A	XP_024301954.1:p.Ser2391Thr
XR_001742208.1:n.8333T>A
XR_002956171.1:n.8279T>A
XR_925644.2:n.8388T>A
NM_001384732.1:c.8164T>A MANE Select	NP_001371661.1:p.Ser2722Thr
NM_023073.4:c.8002T>A	NP_075561.3:p.Ser2668Thr