Canonical Allele Identifier: CA2770491501
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269244_31269264del , CM000668.2:g.31269244_31269264del GRCh38
NC_000006.11:g.31237021_31237041del , CM000668.1:g.31237021_31237041del GRCh37
NC_000006.10:g.31345000_31345020del NCBI36
NG_029422.2:g.7868_7888del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+74_1097-71del MANE Select ENSP00000365402.5:n.1096+74_1097-71del
ENST00000376228.9:c.1096+74_1097-71del ENSP00000365402.5:n.1096+74_1097-71del
ENST00000376237.8:c.*683+74_*684-71del ENSP00000365412.4:n.*683+74_*684-71del
ENST00000383329.7:c.1114+74_1115-71del ENSP00000372819.3:n.1114+74_1115-71del
ENST00000466892.5:n.329+74_330-71del
ENST00000470363.5:n.854+74_855-71del
ENST00000487245.5:n.1455+74_1456-71del
NM_002117.5:c.1096+74_1097-71del NP_002108.4:n.1096+74_1097-71del
NM_002117.6:c.1096+74_1097-71del MANE Select NP_002108.4:n.1096+74_1097-71del