Canonical Allele Identifier: CA1315534

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198755930G>A , CM000663.2:g.198755930G>A	GRCh38
NC_000001.10:g.198725059G>A , CM000663.1:g.198725059G>A	GRCh37
NC_000001.9:g.196991682G>A	NCBI36
NG_007730.1:g.121835G>A
NG_007730.2:g.121836G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.2723G>A
ENST00000697631.1:c.3385G>A	ENSP00000513363.1:p.Val1129Ile
ENST00000697632.1:c.2632G>A	ENSP00000513364.1:p.Val878Ile
ENST00000697633.1:c.2277G>A
ENST00000697635.1:n.623G>A
ENST00000348564.11:c.3187G>A	ENSP00000306782.7:p.Val1063Ile
ENST00000442510.8:c.3670G>A MANE Select	ENSP00000411355.3:p.Val1224Ile
ENST00000348564.10:c.3187G>A	ENSP00000306782.7:p.Val1063Ile
ENST00000442510.6:c.3670G>A	ENSP00000411355.3:p.Val1224Ile
NM_002838.4:c.3670G>A	NP_002829.3:p.Val1224Ile
NM_080921.3:c.3187G>A	NP_563578.2:p.Val1063Ile
XM_006711472.2:c.3526G>A	XP_006711535.1:p.Val1176Ile
XM_006711473.2:c.3472G>A	XP_006711536.1:p.Val1158Ile
XM_006711474.2:c.3328G>A	XP_006711537.1:p.Val1110Ile
XM_006711472.4:c.3526G>A	XP_006711535.1:p.Val1176Ile
XM_006711473.3:c.3472G>A	XP_006711536.1:p.Val1158Ile
XM_006711474.3:c.3328G>A	XP_006711537.1:p.Val1110Ile
NM_002838.5:c.3670G>A MANE Select	NP_002829.3:p.Val1224Ile
NM_080921.4:c.3187G>A	NP_563578.2:p.Val1063Ile