Canonical Allele Identifier: CA2677949809
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269546_31269547del , CM000668.2:g.31269546_31269547del GRCh38
NC_000006.11:g.31237323_31237324del , CM000668.1:g.31237323_31237324del GRCh37
NC_000006.10:g.31345302_31345303del NCBI36
NG_029422.2:g.7586_7587del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-21_1016-20del MANE Select ENSP00000365402.5:n.1016-21_1016-20del
ENST00000376228.9:c.1016-21_1016-20del ENSP00000365402.5:n.1016-21_1016-20del
ENST00000376237.8:c.*603-21_*603-20del ENSP00000365412.4:n.*603-21_*603-20del
ENST00000383329.7:c.1016-3_1016-2del ENSP00000372819.3:n.1016-3_1016-2del
ENST00000466892.5:n.121_122del
ENST00000470363.5:n.753_754del
ENST00000487245.5:n.1375-21_1375-20del
NM_002117.5:c.1016-21_1016-20del NP_002108.4:n.1016-21_1016-20del
NM_002117.6:c.1016-21_1016-20del MANE Select NP_002108.4:n.1016-21_1016-20del