Canonical Allele Identifier: CA1218601710

Gene: PTPRC

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198705436T>G , CM000663.2:g.198705436T>G	GRCh38
NC_000001.10:g.198674565T>G , CM000663.1:g.198674565T>G	GRCh37
NC_000001.9:g.196941188T>G	NCBI36
NG_007730.1:g.71341T>G
NG_007730.2:g.71342T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.1387+938T>G
ENST00000697631.1:c.400+938T>G	ENSP00000513363.1:n.400+938T>G
ENST00000697632.1:c.-354+938T>G	ENSP00000513364.1:n.-354+938T>G
ENST00000348564.11:c.202+938T>G	ENSP00000306782.7:n.202+938T>G
ENST00000367379.6:c.202+938T>G	ENSP00000356349.2:n.202+938T>G
ENST00000442510.8:c.685+938T>G MANE Select	ENSP00000411355.3:n.685+938T>G
ENST00000643513.1:c.343+938T>G	ENSP00000494132.1:n.343+938T>G
ENST00000348564.10:c.202+938T>G	ENSP00000306782.7:n.202+938T>G
ENST00000367367.8:c.487+938T>G	ENSP00000356337.5:n.487+938T>G
ENST00000367379.5:c.202+938T>G	ENSP00000356349.2:n.202+938T>G
ENST00000442510.6:c.685+938T>G	ENSP00000411355.3:n.685+938T>G
ENST00000529828.5:c.541+938T>G	ENSP00000469141.1:n.541+938T>G
ENST00000530727.5:c.343+938T>G	ENSP00000433536.2:n.343+938T>G
NM_002838.4:c.685+938T>G	NP_002829.3:n.685+938T>G
NM_080921.3:c.202+938T>G	NP_563578.2:n.202+938T>G
XM_006711472.2:c.541+938T>G	XP_006711535.1:n.541+938T>G
XM_006711473.2:c.487+938T>G	XP_006711536.1:n.487+938T>G
XM_006711474.2:c.343+938T>G	XP_006711537.1:n.343+938T>G
XM_006711472.4:c.541+938T>G	XP_006711535.1:n.541+938T>G
XM_006711473.3:c.487+938T>G	XP_006711536.1:n.487+938T>G
XM_006711474.3:c.343+938T>G	XP_006711537.1:n.343+938T>G
NM_002838.5:c.685+938T>G MANE Select	NP_002829.3:n.685+938T>G
NM_080921.4:c.202+938T>G	NP_563578.2:n.202+938T>G