Canonical Allele Identifier: CA1314771

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198716687G>A , CM000663.2:g.198716687G>A	GRCh38
NC_000001.10:g.198685816G>A , CM000663.1:g.198685816G>A	GRCh37
NC_000001.9:g.196952439G>A	NCBI36
NG_007730.1:g.82592G>A
NG_007730.2:g.82593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.350G>A
ENST00000697630.1:n.5127G>A
ENST00000697631.1:c.1012G>A	ENSP00000513363.1:p.Asp338Asn
ENST00000697632.1:c.259G>A	ENSP00000513364.1:p.Asp87Asn
ENST00000348564.11:c.814G>A	ENSP00000306782.7:p.Asp272Asn
ENST00000442510.8:c.1297G>A MANE Select	ENSP00000411355.3:p.Asp433Asn
ENST00000348564.10:c.814G>A	ENSP00000306782.7:p.Asp272Asn
ENST00000367367.8:c.1099G>A	ENSP00000356337.5:p.Asp367Asn
ENST00000442510.6:c.1297G>A	ENSP00000411355.3:p.Asp433Asn
ENST00000491302.1:n.289G>A
ENST00000529828.5:c.1153G>A	ENSP00000469141.1:p.Asp385Asn
ENST00000530727.5:c.955G>A	ENSP00000433536.2:p.Asp319Asn
NM_002838.4:c.1297G>A	NP_002829.3:p.Asp433Asn
NM_080921.3:c.814G>A	NP_563578.2:p.Asp272Asn
XM_006711472.2:c.1153G>A	XP_006711535.1:p.Asp385Asn
XM_006711473.2:c.1099G>A	XP_006711536.1:p.Asp367Asn
XM_006711474.2:c.955G>A	XP_006711537.1:p.Asp319Asn
XM_006711472.4:c.1153G>A	XP_006711535.1:p.Asp385Asn
XM_006711473.3:c.1099G>A	XP_006711536.1:p.Asp367Asn
XM_006711474.3:c.955G>A	XP_006711537.1:p.Asp319Asn
NM_002838.5:c.1297G>A MANE Select	NP_002829.3:p.Asp433Asn
NM_080921.4:c.814G>A	NP_563578.2:p.Asp272Asn