Canonical Allele Identifier: CA2677949968
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269686_31269688del , CM000668.2:g.31269686_31269688del GRCh38
NC_000006.11:g.31237463_31237465del , CM000668.1:g.31237463_31237465del GRCh37
NC_000006.10:g.31345442_31345444del NCBI36
NG_029422.2:g.7445_7447del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-162_1016-160del MANE Select ENSP00000365402.5:n.1016-162_1016-160del
ENST00000376228.9:c.1016-162_1016-160del ENSP00000365402.5:n.1016-162_1016-160del
ENST00000376237.8:c.*603-162_*603-160del ENSP00000365412.4:n.*603-162_*603-160del
ENST00000383329.7:c.1016-144_1016-142del ENSP00000372819.3:n.1016-144_1016-142del
ENST00000470363.5:n.612_614del
ENST00000487245.5:n.1375-162_1375-160del
NM_002117.5:c.1016-162_1016-160del NP_002108.4:n.1016-162_1016-160del
NM_002117.6:c.1016-162_1016-160del MANE Select NP_002108.4:n.1016-162_1016-160del