Canonical Allele Identifier: CA1619080582
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761338304

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271383_31271384insACCCC , CM000668.2:g.31271383_31271384insACCCC GRCh38
NC_000006.11:g.31239160_31239161insACCCC , CM000668.1:g.31239160_31239161insACCCC GRCh37
NC_000006.10:g.31347139_31347140insACCCC NCBI36
NG_029422.2:g.5748_5749insGGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-36_344-35insGGGGT MANE Select ENSP00000365402.5:n.344-36_344-35insGGGGT
ENST00000376228.9:c.344-36_344-35insGGGGT ENSP00000365402.5:n.344-36_344-35insGGGGT
ENST00000376237.8:c.344-53_344-52insGGGGT ENSP00000365412.4:n.344-53_344-52insGGGGT
ENST00000383329.7:c.344-36_344-35insGGGGT ENSP00000372819.3:n.344-36_344-35insGGGGT
ENST00000415537.1:c.342-36_342-35insGGGGT
ENST00000484378.1:n.577_578insGGGGT
ENST00000487245.5:n.667_668insGGGGT
ENST00000495835.1:n.533-36_533-35insGGGGT
NM_002117.5:c.344-36_344-35insGGGGT NP_002108.4:n.344-36_344-35insGGGGT
NM_002117.6:c.344-36_344-35insGGGGT MANE Select NP_002108.4:n.344-36_344-35insGGGGT