Canonical Allele Identifier: CA344054922

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198752728A>C , CM000663.2:g.198752728A>C	GRCh38
NC_000001.10:g.198721857A>C , CM000663.1:g.198721857A>C	GRCh37
NC_000001.9:g.196988480A>C	NCBI36
NG_007730.1:g.118633A>C
NG_007730.2:g.118634A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.2518A>C
ENST00000697631.1:c.3180A>C	ENSP00000513363.1:p.Glu1060Asp
ENST00000697632.1:c.2427A>C	ENSP00000513364.1:p.Glu809Asp
ENST00000697633.1:c.2072A>C
ENST00000697634.1:n.1622A>C
ENST00000697635.1:n.418A>C
ENST00000348564.11:c.2982A>C	ENSP00000306782.7:p.Glu994Asp
ENST00000442510.8:c.3465A>C MANE Select	ENSP00000411355.3:p.Glu1155Asp
ENST00000646230.1:n.374A>C
ENST00000348564.10:c.2982A>C	ENSP00000306782.7:p.Glu994Asp
ENST00000442510.6:c.3465A>C	ENSP00000411355.3:p.Glu1155Asp
NM_002838.4:c.3465A>C	NP_002829.3:p.Glu1155Asp
NM_080921.3:c.2982A>C	NP_563578.2:p.Glu994Asp
XM_006711472.2:c.3321A>C	XP_006711535.1:p.Glu1107Asp
XM_006711473.2:c.3267A>C	XP_006711536.1:p.Glu1089Asp
XM_006711474.2:c.3123A>C	XP_006711537.1:p.Glu1041Asp
XM_006711472.4:c.3321A>C	XP_006711535.1:p.Glu1107Asp
XM_006711473.3:c.3267A>C	XP_006711536.1:p.Glu1089Asp
XM_006711474.3:c.3123A>C	XP_006711537.1:p.Glu1041Asp
NM_002838.5:c.3465A>C MANE Select	NP_002829.3:p.Glu1155Asp
NM_080921.4:c.2982A>C	NP_563578.2:p.Glu994Asp