Canonical Allele Identifier: CA344039534
Gene: PTPRC HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000491302.2:n.677A>C
ENST00000697630.1:n.5454A>C
ENST00000697631.1:c.1339A>C ENSP00000513363.1:p.Lys447Gln
ENST00000697632.1:c.586A>C ENSP00000513364.1:p.Lys196Gln
ENST00000697633.1:c.99A>C
ENST00000348564.11:c.1141A>C ENSP00000306782.7:p.Lys381Gln
ENST00000442510.8:c.1624A>C MANE Select ENSP00000411355.3:p.Lys542Gln
ENST00000348564.10:c.1141A>C ENSP00000306782.7:p.Lys381Gln
ENST00000367367.8:c.1426A>C ENSP00000356337.5:p.Lys476Gln
ENST00000442510.6:c.1624A>C ENSP00000411355.3:p.Lys542Gln
ENST00000491302.1:n.616A>C
ENST00000529828.5:c.1480A>C ENSP00000469141.1:p.Lys494Gln
ENST00000530727.5:c.1282A>C ENSP00000433536.2:p.Lys428Gln
NM_002838.4:c.1624A>C NP_002829.3:p.Lys542Gln
NM_080921.3:c.1141A>C NP_563578.2:p.Lys381Gln
XM_006711472.2:c.1480A>C XP_006711535.1:p.Lys494Gln
XM_006711473.2:c.1426A>C XP_006711536.1:p.Lys476Gln
XM_006711474.2:c.1282A>C XP_006711537.1:p.Lys428Gln
XM_006711472.4:c.1480A>C XP_006711535.1:p.Lys494Gln
XM_006711473.3:c.1426A>C XP_006711536.1:p.Lys476Gln
XM_006711474.3:c.1282A>C XP_006711537.1:p.Lys428Gln
NM_002838.5:c.1624A>C MANE Select NP_002829.3:p.Lys542Gln
NM_080921.4:c.1141A>C NP_563578.2:p.Lys381Gln