Canonical Allele Identifier: CA2677951267
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271150_31271151insCG , CM000668.2:g.31271150_31271151insCG GRCh38
NC_000006.11:g.31238927_31238928insCG , CM000668.1:g.31238927_31238928insCG GRCh37
NC_000006.10:g.31346906_31346907insCG NCBI36
NG_029422.2:g.5981_5982insCG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.541_542insCG MANE Select ENSP00000365402.5:p.Arg181ThrfsTer?
ENST00000376228.9:c.541_542insCG ENSP00000365402.5:p.Arg181ThrfsTer?
ENST00000376237.8:c.*128_*129insCG ENSP00000365412.4:n.*128_*129insCG
ENST00000383329.7:c.541_542insCG ENSP00000372819.3:p.Arg181ThrfsTer?
ENST00000415537.1:c.539_540insCG
ENST00000484378.1:n.810_811insCG
ENST00000487245.5:n.900_901insCG
ENST00000495835.1:n.730_731insCG
NM_002117.5:c.541_542insCG NP_002108.4:p.Arg181ThrfsTer?
NM_002117.6:c.541_542insCG MANE Select NP_002108.4:p.Arg181ThrfsTer?