Canonical Allele Identifier: CA1140224183

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198731313G= , CM000663.2:g.198731313G=	GRCh38
NC_000001.10:g.198700442G= , CM000663.1:g.198700442G=	GRCh37
NC_000001.9:g.196967065G=	NCBI36
NG_007730.1:g.97218G=
NG_007730.2:g.97219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.918-304G=
ENST00000697630.1:n.5695-304G=
ENST00000697631.1:c.1580-304G=	ENSP00000513363.1:n.1580-304G=
ENST00000697632.1:c.827-304G=	ENSP00000513364.1:n.827-304G=
ENST00000697633.1:c.472-304G=
ENST00000348564.11:c.1382-304G=	ENSP00000306782.7:n.1382-304G=
ENST00000442510.8:c.1865-304G= MANE Select	ENSP00000411355.3:n.1865-304G=
ENST00000348564.10:c.1382-304G=	ENSP00000306782.7:n.1382-304G=
ENST00000367367.8:c.1667-304G=	ENSP00000356337.5:n.1667-304G=
ENST00000442510.6:c.1865-304G=	ENSP00000411355.3:n.1865-304G=
ENST00000529828.5:c.1721-304G=	ENSP00000469141.1:n.1721-304G=
ENST00000530727.5:c.1523-304G=	ENSP00000433536.2:n.1523-304G=
NM_002838.4:c.1865-304G=	NP_002829.3:n.1865-304G=
NM_080921.3:c.1382-304G=	NP_563578.2:n.1382-304G=
XM_006711472.2:c.1721-304G=	XP_006711535.1:n.1721-304G=
XM_006711473.2:c.1667-304G=	XP_006711536.1:n.1667-304G=
XM_006711474.2:c.1523-304G=	XP_006711537.1:n.1523-304G=
XM_006711472.4:c.1721-304G=	XP_006711535.1:n.1721-304G=
XM_006711473.3:c.1667-304G=	XP_006711536.1:n.1667-304G=
XM_006711474.3:c.1523-304G=	XP_006711537.1:n.1523-304G=
NM_002838.5:c.1865-304G= MANE Select	NP_002829.3:n.1865-304G=
NM_080921.4:c.1382-304G=	NP_563578.2:n.1382-304G=