Canonical Allele Identifier: CA1619077790
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269397_31269398delinsCA , CM000668.2:g.31269397_31269398delinsCA GRCh38
NC_000006.11:g.31237174_31237175delinsCA , CM000668.1:g.31237174_31237175delinsCA GRCh37
NC_000006.10:g.31345153_31345154delinsCA NCBI36
NG_029422.2:g.7734_7735delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-13_1049-12delinsTG MANE Select ENSP00000365402.5:n.1049-13_1049-12delinsTG
ENST00000376228.9:c.1049-13_1049-12delinsTG ENSP00000365402.5:n.1049-13_1049-12delinsTG
ENST00000376237.8:c.*636-13_*636-12delinsTG ENSP00000365412.4:n.*636-13_*636-12delinsTG
ENST00000383329.7:c.1067-13_1067-12delinsTG ENSP00000372819.3:n.1067-13_1067-12delinsTG
ENST00000466892.5:n.269_270delinsTG
ENST00000470363.5:n.807-13_807-12delinsTG
ENST00000487245.5:n.1408-13_1408-12delinsTG
NM_002117.5:c.1049-13_1049-12delinsTG NP_002108.4:n.1049-13_1049-12delinsTG
NM_002117.6:c.1049-13_1049-12delinsTG MANE Select NP_002108.4:n.1049-13_1049-12delinsTG