Canonical Allele Identifier: CA144640

Gene: PTPRC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198718267A>T , CM000663.2:g.198718267A>T	GRCh38
NC_000001.10:g.198687396A>T , CM000663.1:g.198687396A>T	GRCh37
NC_000001.9:g.196954019A>T	NCBI36
NG_007730.1:g.84172A>T
NG_007730.2:g.84173A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.677A>T
ENST00000697630.1:n.5454A>T
ENST00000697631.1:c.1339A>T	ENSP00000513363.1:p.Lys447Ter
ENST00000697632.1:c.586A>T	ENSP00000513364.1:p.Lys196Ter
ENST00000697633.1:c.99A>T
ENST00000348564.11:c.1141A>T	ENSP00000306782.7:p.Lys381Ter
ENST00000442510.8:c.1624A>T MANE Select	ENSP00000411355.3:p.Lys542Ter
ENST00000348564.10:c.1141A>T	ENSP00000306782.7:p.Lys381Ter
ENST00000367367.8:c.1426A>T	ENSP00000356337.5:p.Lys476Ter
ENST00000442510.6:c.1624A>T	ENSP00000411355.3:p.Lys542Ter
ENST00000491302.1:n.616A>T
ENST00000529828.5:c.1480A>T	ENSP00000469141.1:p.Lys494Ter
ENST00000530727.5:c.1282A>T	ENSP00000433536.2:p.Lys428Ter
NM_002838.4:c.1624A>T	NP_002829.3:p.Lys542Ter
NM_080921.3:c.1141A>T	NP_563578.2:p.Lys381Ter
XM_006711472.2:c.1480A>T	XP_006711535.1:p.Lys494Ter
XM_006711473.2:c.1426A>T	XP_006711536.1:p.Lys476Ter
XM_006711474.2:c.1282A>T	XP_006711537.1:p.Lys428Ter
XM_006711472.4:c.1480A>T	XP_006711535.1:p.Lys494Ter
XM_006711473.3:c.1426A>T	XP_006711536.1:p.Lys476Ter
XM_006711474.3:c.1282A>T	XP_006711537.1:p.Lys428Ter
NM_002838.5:c.1624A>T MANE Select	NP_002829.3:p.Lys542Ter
NM_080921.4:c.1141A>T	NP_563578.2:p.Lys381Ter