Canonical Allele Identifier: CA2677951272
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271151_31271152insAT , CM000668.2:g.31271151_31271152insAT GRCh38
NC_000006.11:g.31238928_31238929insAT , CM000668.1:g.31238928_31238929insAT GRCh37
NC_000006.10:g.31346907_31346908insAT NCBI36
NG_029422.2:g.5981_5982insTA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.541_542insTA MANE Select ENSP00000365402.5:p.Arg181IlefsTer?
ENST00000376228.9:c.541_542insTA ENSP00000365402.5:p.Arg181IlefsTer?
ENST00000376237.8:c.*128_*129insTA ENSP00000365412.4:n.*128_*129insTA
ENST00000383329.7:c.541_542insTA ENSP00000372819.3:p.Arg181IlefsTer?
ENST00000415537.1:c.539_540insTA
ENST00000484378.1:n.810_811insTA
ENST00000487245.5:n.900_901insTA
ENST00000495835.1:n.730_731insTA
NM_002117.5:c.541_542insTA NP_002108.4:p.Arg181IlefsTer?
NM_002117.6:c.541_542insTA MANE Select NP_002108.4:p.Arg181IlefsTer?