Canonical Allele Identifier: CA1315129
Gene: PTPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198741955G>C , CM000663.2:g.198741955G>C GRCh38
NC_000001.10:g.198711084G>C , CM000663.1:g.198711084G>C GRCh37
NC_000001.9:g.196977707G>C NCBI36
NG_007730.1:g.107860G>C
NG_007730.2:g.107861G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000491302.2:n.1543G>C
ENST00000697630.1:n.6320G>C
ENST00000697631.1:c.2205G>C ENSP00000513363.1:p.Leu735Phe
ENST00000697632.1:c.1452G>C ENSP00000513364.1:p.Leu484Phe
ENST00000697633.1:c.1097G>C
ENST00000348564.11:c.2007G>C ENSP00000306782.7:p.Leu669Phe
ENST00000442510.8:c.2490G>C MANE Select ENSP00000411355.3:p.Leu830Phe
ENST00000348564.10:c.2007G>C ENSP00000306782.7:p.Leu669Phe
ENST00000442510.6:c.2490G>C ENSP00000411355.3:p.Leu830Phe
NM_002838.4:c.2490G>C NP_002829.3:p.Leu830Phe
NM_080921.3:c.2007G>C NP_563578.2:p.Leu669Phe
XM_006711472.2:c.2346G>C XP_006711535.1:p.Leu782Phe
XM_006711473.2:c.2292G>C XP_006711536.1:p.Leu764Phe
XM_006711474.2:c.2148G>C XP_006711537.1:p.Leu716Phe
XM_006711472.4:c.2346G>C XP_006711535.1:p.Leu782Phe
XM_006711473.3:c.2292G>C XP_006711536.1:p.Leu764Phe
XM_006711474.3:c.2148G>C XP_006711537.1:p.Leu716Phe
NM_002838.5:c.2490G>C MANE Select NP_002829.3:p.Leu830Phe
NM_080921.4:c.2007G>C NP_563578.2:p.Leu669Phe