Canonical Allele Identifier: CA292980

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198699632G>C , CM000663.2:g.198699632G>C	GRCh38
NC_000001.10:g.198668761G>C , CM000663.1:g.198668761G>C	GRCh37
NC_000001.9:g.196935384G>C	NCBI36
NG_007730.1:g.65537G>C
NG_007730.2:g.65538G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.187-3666G>C
ENST00000697631.1:c.298+2723G>C	ENSP00000513363.1:n.298+2723G>C
ENST00000697632.1:c.-455-3666G>C	ENSP00000513364.1:n.-455-3666G>C
ENST00000348564.11:c.101-3666G>C	ENSP00000306782.7:n.101-3666G>C
ENST00000367379.6:c.101-3666G>C	ENSP00000356349.2:n.101-3666G>C
ENST00000442510.8:c.367G>C MANE Select	ENSP00000411355.3:p.Asp123His
ENST00000643513.1:c.169G>C	ENSP00000494132.1:p.Asp57His
ENST00000645247.1:c.292G>C	ENSP00000494327.1:p.Asp98His
ENST00000348564.10:c.101-3666G>C	ENSP00000306782.7:n.101-3666G>C
ENST00000367367.8:c.169G>C	ENSP00000356337.5:p.Asp57His
ENST00000367379.5:c.101-3666G>C	ENSP00000356349.2:n.101-3666G>C
ENST00000391970.3:n.143G>C
ENST00000427110.6:n.143G>C
ENST00000442510.6:c.367G>C	ENSP00000411355.3:p.Asp123His
ENST00000462363.6:n.277G>C
ENST00000484135.1:n.98G>C
ENST00000529828.5:c.367G>C	ENSP00000469141.1:p.Asp123His
ENST00000530727.5:c.169G>C	ENSP00000433536.2:p.Asp57His
NM_002838.4:c.367G>C	NP_002829.3:p.Asp123His
NM_080921.3:c.101-3666G>C	NP_563578.2:n.101-3666G>C
XM_006711472.2:c.367G>C	XP_006711535.1:p.Asp123His
XM_006711473.2:c.169G>C	XP_006711536.1:p.Asp57His
XM_006711474.2:c.169G>C	XP_006711537.1:p.Asp57His
XM_006711472.4:c.367G>C	XP_006711535.1:p.Asp123His
XM_006711473.3:c.169G>C	XP_006711536.1:p.Asp57His
XM_006711474.3:c.169G>C	XP_006711537.1:p.Asp57His
NM_002838.5:c.367G>C MANE Select	NP_002829.3:p.Asp123His
NM_080921.4:c.101-3666G>C	NP_563578.2:n.101-3666G>C