Canonical Allele Identifier: CA2677949587
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269279_31269280del , CM000668.2:g.31269279_31269280del GRCh38
NC_000006.11:g.31237056_31237057del , CM000668.1:g.31237056_31237057del GRCh37
NC_000006.10:g.31345035_31345036del NCBI36
NG_029422.2:g.7852_7853del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+58_1096+59del MANE Select ENSP00000365402.5:n.1096+58_1096+59del
ENST00000376228.9:c.1096+58_1096+59del ENSP00000365402.5:n.1096+58_1096+59del
ENST00000376237.8:c.*683+58_*683+59del ENSP00000365412.4:n.*683+58_*683+59del
ENST00000383329.7:c.1114+58_1114+59del ENSP00000372819.3:n.1114+58_1114+59del
ENST00000466892.5:n.329+58_329+59del
ENST00000470363.5:n.854+58_854+59del
ENST00000487245.5:n.1455+58_1455+59del
NM_002117.5:c.1096+58_1096+59del NP_002108.4:n.1096+58_1096+59del
NM_002117.6:c.1096+58_1096+59del MANE Select NP_002108.4:n.1096+58_1096+59del