Canonical Allele Identifier: CA1141436199

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198754304T= , CM000663.2:g.198754304T=	GRCh38
NC_000001.10:g.198723433T= , CM000663.1:g.198723433T=	GRCh37
NC_000001.9:g.196990056T=	NCBI36
NG_007730.1:g.120209T=
NG_007730.2:g.120210T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002838.5:c.3545T= MANE Select	NP_002829.3:p.Leu1182=
ENST00000442510.8:c.3545T= MANE Select	ENSP00000411355.3:p.Leu1182=
NM_002838.4:c.3545T=	NP_002829.3:p.Leu1182=
NM_080921.3:c.3062T=	NP_563578.2:p.Leu1021=
NM_080921.4:c.3062T=	NP_563578.2:p.Leu1021=
ENST00000348564.10:c.3062T=	ENSP00000306782.7:p.Leu1021=
ENST00000348564.11:c.3062T=	ENSP00000306782.7:p.Leu1021=
ENST00000442510.6:c.3545T=	ENSP00000411355.3:p.Leu1182=
ENST00000491302.2:n.2598T=
ENST00000646230.1:n.454T=
ENST00000697631.1:c.3260T=	ENSP00000513363.1:p.Leu1087=
ENST00000697632.1:c.2507T=	ENSP00000513364.1:p.Leu836=
ENST00000697633.1:c.2152T=
ENST00000697635.1:n.498T=
XM_006711472.2:c.3401T=	XP_006711535.1:p.Leu1134=
XM_006711472.4:c.3401T=	XP_006711535.1:p.Leu1134=
XM_006711473.2:c.3347T=	XP_006711536.1:p.Leu1116=
XM_006711473.3:c.3347T=	XP_006711536.1:p.Leu1116=
XM_006711474.2:c.3203T=	XP_006711537.1:p.Leu1068=
XM_006711474.3:c.3203T=	XP_006711537.1:p.Leu1068=