Canonical Allele Identifier: CA1314657

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198708210A>G , CM000663.2:g.198708210A>G	GRCh38
NC_000001.10:g.198677339A>G , CM000663.1:g.198677339A>G	GRCh37
NC_000001.9:g.196943962A>G	NCBI36
NG_007730.1:g.74115A>G
NG_007730.2:g.74116A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.1684A>G
ENST00000697631.1:c.697A>G	ENSP00000513363.1:p.Ile233Val
ENST00000697632.1:c.-57A>G	ENSP00000513364.1:n.-57A>G
ENST00000348564.11:c.499A>G	ENSP00000306782.7:p.Ile167Val
ENST00000442510.8:c.982A>G MANE Select	ENSP00000411355.3:p.Ile328Val
ENST00000348564.10:c.499A>G	ENSP00000306782.7:p.Ile167Val
ENST00000367367.8:c.784A>G	ENSP00000356337.5:p.Ile262Val
ENST00000442510.6:c.982A>G	ENSP00000411355.3:p.Ile328Val
ENST00000529828.5:c.838A>G	ENSP00000469141.1:p.Ile280Val
ENST00000530727.5:c.640A>G	ENSP00000433536.2:p.Ile214Val
NM_002838.4:c.982A>G	NP_002829.3:p.Ile328Val
NM_080921.3:c.499A>G	NP_563578.2:p.Ile167Val
XM_006711472.2:c.838A>G	XP_006711535.1:p.Ile280Val
XM_006711473.2:c.784A>G	XP_006711536.1:p.Ile262Val
XM_006711474.2:c.640A>G	XP_006711537.1:p.Ile214Val
XM_006711472.4:c.838A>G	XP_006711535.1:p.Ile280Val
XM_006711473.3:c.784A>G	XP_006711536.1:p.Ile262Val
XM_006711474.3:c.640A>G	XP_006711537.1:p.Ile214Val
NM_002838.5:c.982A>G MANE Select	NP_002829.3:p.Ile328Val
NM_080921.4:c.499A>G	NP_563578.2:p.Ile167Val