Canonical Allele Identifier: CA1314524

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198702513T>A , CM000663.2:g.198702513T>A	GRCh38
NC_000001.10:g.198671642T>A , CM000663.1:g.198671642T>A	GRCh37
NC_000001.9:g.196938265T>A	NCBI36
NG_007730.1:g.68418T>A
NG_007730.2:g.68419T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.187-785T>A
ENST00000697631.1:c.299-785T>A	ENSP00000513363.1:n.299-785T>A
ENST00000697632.1:c.-455-785T>A	ENSP00000513364.1:n.-455-785T>A
ENST00000348564.11:c.101-785T>A	ENSP00000306782.7:n.101-785T>A
ENST00000367379.6:c.101-785T>A	ENSP00000356349.2:n.101-785T>A
ENST00000442510.8:c.566T>A MANE Select	ENSP00000411355.3:p.Ile189Asn
ENST00000643513.1:c.242-785T>A	ENSP00000494132.1:n.242-785T>A
ENST00000645247.1:c.365-785T>A	ENSP00000494327.1:n.365-785T>A
ENST00000348564.10:c.101-785T>A	ENSP00000306782.7:n.101-785T>A
ENST00000367367.8:c.368T>A	ENSP00000356337.5:p.Ile123Asn
ENST00000367379.5:c.101-785T>A	ENSP00000356349.2:n.101-785T>A
ENST00000391970.3:n.342T>A
ENST00000427110.6:n.216-785T>A
ENST00000442510.6:c.566T>A	ENSP00000411355.3:p.Ile189Asn
ENST00000462363.6:n.350-785T>A
ENST00000529828.5:c.440-785T>A	ENSP00000469141.1:n.440-785T>A
ENST00000530727.5:c.242-785T>A	ENSP00000433536.2:n.242-785T>A
NM_002838.4:c.566T>A	NP_002829.3:p.Ile189Asn
NM_080921.3:c.101-785T>A	NP_563578.2:n.101-785T>A
XM_006711472.2:c.440-785T>A	XP_006711535.1:n.440-785T>A
XM_006711473.2:c.368T>A	XP_006711536.1:p.Ile123Asn
XM_006711474.2:c.242-785T>A	XP_006711537.1:n.242-785T>A
XM_006711472.4:c.440-785T>A	XP_006711535.1:n.440-785T>A
XM_006711473.3:c.368T>A	XP_006711536.1:p.Ile123Asn
XM_006711474.3:c.242-785T>A	XP_006711537.1:n.242-785T>A
NM_002838.5:c.566T>A MANE Select	NP_002829.3:p.Ile189Asn
NM_080921.4:c.101-785T>A	NP_563578.2:n.101-785T>A