Canonical Allele Identifier: CA2677949157
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268941_31268942del , CM000668.2:g.31268941_31268942del GRCh38
NC_000006.11:g.31236718_31236719del , CM000668.1:g.31236718_31236719del GRCh37
NC_000006.10:g.31344697_31344698del NCBI36
NG_029422.2:g.8192_8193del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*229_*230del MANE Select ENSP00000365402.5:n.*229_*230del
ENST00000376228.9:c.*229_*230del ENSP00000365402.5:n.*229_*230del
ENST00000376237.8:c.*917_*918del ENSP00000365412.4:n.*917_*918del
ENST00000383329.7:c.*229_*230del ENSP00000372819.3:n.*229_*230del
ENST00000466892.5:n.563_564del
ENST00000470363.5:n.1088_1089del
ENST00000487245.5:n.1689_1690del
NM_002117.5:c.*229_*230del NP_002108.4:n.*229_*230del
NM_002117.6:c.*229_*230del MANE Select NP_002108.4:n.*229_*230del