Canonical Allele Identifier: CA1314655

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198708161T>C , CM000663.2:g.198708161T>C	GRCh38
NC_000001.10:g.198677290T>C , CM000663.1:g.198677290T>C	GRCh37
NC_000001.9:g.196943913T>C	NCBI36
NG_007730.1:g.74066T>C
NG_007730.2:g.74067T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.1635T>C
ENST00000697631.1:c.648T>C	ENSP00000513363.1:p.Cys216=
ENST00000697632.1:c.-106T>C	ENSP00000513364.1:n.-106T>C
ENST00000348564.11:c.450T>C	ENSP00000306782.7:p.Cys150=
ENST00000442510.8:c.933T>C MANE Select	ENSP00000411355.3:p.Cys311=
ENST00000348564.10:c.450T>C	ENSP00000306782.7:p.Cys150=
ENST00000367367.8:c.735T>C	ENSP00000356337.5:p.Cys245=
ENST00000442510.6:c.933T>C	ENSP00000411355.3:p.Cys311=
ENST00000529828.5:c.789T>C	ENSP00000469141.1:p.Cys263=
ENST00000530727.5:c.591T>C	ENSP00000433536.2:p.Cys197=
NM_002838.4:c.933T>C	NP_002829.3:p.Cys311=
NM_080921.3:c.450T>C	NP_563578.2:p.Cys150=
XM_006711472.2:c.789T>C	XP_006711535.1:p.Cys263=
XM_006711473.2:c.735T>C	XP_006711536.1:p.Cys245=
XM_006711474.2:c.591T>C	XP_006711537.1:p.Cys197=
XM_006711472.4:c.789T>C	XP_006711535.1:p.Cys263=
XM_006711473.3:c.735T>C	XP_006711536.1:p.Cys245=
XM_006711474.3:c.591T>C	XP_006711537.1:p.Cys197=
NM_002838.5:c.933T>C MANE Select	NP_002829.3:p.Cys311=
NM_080921.4:c.450T>C	NP_563578.2:p.Cys150=