Canonical Allele Identifier: CA2677949632
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269326_31269327del , CM000668.2:g.31269326_31269327del GRCh38
NC_000006.11:g.31237103_31237104del , CM000668.1:g.31237103_31237104del GRCh37
NC_000006.10:g.31345082_31345083del NCBI36
NG_029422.2:g.7807_7808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+13_1096+14del MANE Select ENSP00000365402.5:n.1096+13_1096+14del
ENST00000376228.9:c.1096+13_1096+14del ENSP00000365402.5:n.1096+13_1096+14del
ENST00000376237.8:c.*683+13_*683+14del ENSP00000365412.4:n.*683+13_*683+14del
ENST00000383329.7:c.1114+13_1114+14del ENSP00000372819.3:n.1114+13_1114+14del
ENST00000466892.5:n.329+13_329+14del
ENST00000470363.5:n.854+13_854+14del
ENST00000487245.5:n.1455+13_1455+14del
NM_002117.5:c.1096+13_1096+14del NP_002108.4:n.1096+13_1096+14del
NM_002117.6:c.1096+13_1096+14del MANE Select NP_002108.4:n.1096+13_1096+14del