Canonical Allele Identifier: CA2677949812
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269547_31269548dup , CM000668.2:g.31269547_31269548dup GRCh38
NC_000006.11:g.31237324_31237325dup , CM000668.1:g.31237324_31237325dup GRCh37
NC_000006.10:g.31345303_31345304dup NCBI36
NG_029422.2:g.7584_7585dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-23_1016-22dup MANE Select ENSP00000365402.5:n.1016-23_1016-22dup
ENST00000376228.9:c.1016-23_1016-22dup ENSP00000365402.5:n.1016-23_1016-22dup
ENST00000376237.8:c.*603-23_*603-22dup ENSP00000365412.4:n.*603-23_*603-22dup
ENST00000383329.7:c.1016-5_1016-4dup ENSP00000372819.3:n.1016-5_1016-4dup
ENST00000466892.5:n.119_120dup
ENST00000470363.5:n.751_752dup
ENST00000487245.5:n.1375-23_1375-22dup
NM_002117.5:c.1016-23_1016-22dup NP_002108.4:n.1016-23_1016-22dup
NM_002117.6:c.1016-23_1016-22dup MANE Select NP_002108.4:n.1016-23_1016-22dup