Canonical Allele Identifier: CA1619080251
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271026_31271027delinsCG , CM000668.2:g.31271026_31271027delinsCG GRCh38
NC_000006.11:g.31238803_31238804delinsCG , CM000668.1:g.31238803_31238804delinsCG GRCh37
NC_000006.10:g.31346782_31346783delinsCG NCBI36
NG_029422.2:g.6105_6106delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+46_619+47delinsCG MANE Select ENSP00000365402.5:n.619+46_619+47delinsCG...
ENST00000376228.9:c.619+46_619+47delinsCG ENSP00000365402.5:n.619+46_619+47delinsCG...
ENST00000376237.8:c.*206+46_*206+47delinsCG ENSP00000365412.4:n.*206+46_*206+47delins...
ENST00000383329.7:c.619+46_619+47delinsCG ENSP00000372819.3:n.619+46_619+47delinsCG...
ENST00000415537.1:c.617+46_617+47delinsCG
ENST00000487245.5:n.978+46_978+47delinsCG
ENST00000495835.1:n.808+46_808+47delinsCG
NM_002117.5:c.619+46_619+47delinsCG NP_002108.4:n.619+46_619+47delinsCG
NM_002117.6:c.619+46_619+47delinsCG MANE Select NP_002108.4:n.619+46_619+47delinsCG