Canonical Allele Identifier: CA1315350

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198750486A>G , CM000663.2:g.198750486A>G	GRCh38
NC_000001.10:g.198719615A>G , CM000663.1:g.198719615A>G	GRCh37
NC_000001.9:g.196986238A>G	NCBI36
NG_007730.1:g.116391A>G
NG_007730.2:g.116392A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002838.5:c.3073-6A>G MANE Select	NP_002829.3:n.3073-6A>G
ENST00000442510.8:c.3073-6A>G MANE Select	ENSP00000411355.3:n.3073-6A>G
NM_002838.4:c.3073-6A>G	NP_002829.3:n.3073-6A>G
NM_080921.3:c.2590-6A>G	NP_563578.2:n.2590-6A>G
NM_080921.4:c.2590-6A>G	NP_563578.2:n.2590-6A>G
ENST00000348564.10:c.2590-6A>G	ENSP00000306782.7:n.2590-6A>G
ENST00000348564.11:c.2590-6A>G	ENSP00000306782.7:n.2590-6A>G
ENST00000442510.6:c.3073-6A>G	ENSP00000411355.3:n.3073-6A>G
ENST00000491302.2:n.2126-6A>G
ENST00000697631.1:c.2788-6A>G	ENSP00000513363.1:n.2788-6A>G
ENST00000697632.1:c.2035-6A>G	ENSP00000513364.1:n.2035-6A>G
ENST00000697633.1:c.1680-6A>G
XM_006711472.2:c.2929-6A>G	XP_006711535.1:n.2929-6A>G
XM_006711472.4:c.2929-6A>G	XP_006711535.1:n.2929-6A>G
XM_006711473.2:c.2875-6A>G	XP_006711536.1:n.2875-6A>G
XM_006711473.3:c.2875-6A>G	XP_006711536.1:n.2875-6A>G
XM_006711474.2:c.2731-6A>G	XP_006711537.1:n.2731-6A>G
XM_006711474.3:c.2731-6A>G	XP_006711537.1:n.2731-6A>G