Canonical Allele Identifier: CA1619080674
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271527_31271528delinsTC , CM000668.2:g.31271527_31271528delinsTC GRCh38
NC_000006.11:g.31239304_31239305delinsTC , CM000668.1:g.31239304_31239305delinsTC GRCh37
NC_000006.10:g.31347283_31347284delinsTC NCBI36
NG_029422.2:g.5604_5605delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+71_343+72delinsGA MANE Select ENSP00000365402.5:n.343+71_343+72delinsGA
ENST00000376228.9:c.343+71_343+72delinsGA ENSP00000365402.5:n.343+71_343+72delinsGA
ENST00000376237.8:c.343+71_343+72delinsGA ENSP00000365412.4:n.343+71_343+72delinsGA
ENST00000383329.7:c.343+71_343+72delinsGA ENSP00000372819.3:n.343+71_343+72delinsGA
ENST00000415537.1:c.341+71_341+72delinsGA
ENST00000484378.1:n.433_434delinsGA
ENST00000487245.5:n.523_524delinsGA
ENST00000495835.1:n.532+71_532+72delinsGA
NM_002117.5:c.343+71_343+72delinsGA NP_002108.4:n.343+71_343+72delinsGA
NM_002117.6:c.343+71_343+72delinsGA MANE Select NP_002108.4:n.343+71_343+72delinsGA