Canonical Allele Identifier: CA344041115

Gene: PTPRC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198722466T>G , CM000663.2:g.198722466T>G	GRCh38
NC_000001.10:g.198691595T>G , CM000663.1:g.198691595T>G	GRCh37
NC_000001.9:g.196958218T>G	NCBI36
NG_007730.1:g.88371T>G
NG_007730.2:g.88372T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.763T>G
ENST00000697630.1:n.5540T>G
ENST00000697631.1:c.1425T>G	ENSP00000513363.1:p.His475Gln
ENST00000697632.1:c.672T>G	ENSP00000513364.1:p.His224Gln
ENST00000697633.1:c.185T>G
ENST00000348564.11:c.1227T>G	ENSP00000306782.7:p.His409Gln
ENST00000442510.8:c.1710T>G MANE Select	ENSP00000411355.3:p.His570Gln
ENST00000348564.10:c.1227T>G	ENSP00000306782.7:p.His409Gln
ENST00000367367.8:c.1512T>G	ENSP00000356337.5:p.His504Gln
ENST00000442510.6:c.1710T>G	ENSP00000411355.3:p.His570Gln
ENST00000529828.5:c.1566T>G	ENSP00000469141.1:p.His522Gln
ENST00000530727.5:c.1368T>G	ENSP00000433536.2:p.His456Gln
NM_002838.4:c.1710T>G	NP_002829.3:p.His570Gln
NM_080921.3:c.1227T>G	NP_563578.2:p.His409Gln
XM_006711472.2:c.1566T>G	XP_006711535.1:p.His522Gln
XM_006711473.2:c.1512T>G	XP_006711536.1:p.His504Gln
XM_006711474.2:c.1368T>G	XP_006711537.1:p.His456Gln
XM_006711472.4:c.1566T>G	XP_006711535.1:p.His522Gln
XM_006711473.3:c.1512T>G	XP_006711536.1:p.His504Gln
XM_006711474.3:c.1368T>G	XP_006711537.1:p.His456Gln
NM_002838.5:c.1710T>G MANE Select	NP_002829.3:p.His570Gln
NM_080921.4:c.1227T>G	NP_563578.2:p.His409Gln