Canonical Allele Identifier: CA2677951663
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271577_31271578del , CM000668.2:g.31271577_31271578del GRCh38
NC_000006.11:g.31239354_31239355del , CM000668.1:g.31239354_31239355del GRCh37
NC_000006.10:g.31347333_31347334del NCBI36
NG_029422.2:g.5556_5557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+23_343+24del MANE Select ENSP00000365402.5:n.343+23_343+24del
ENST00000376228.9:c.343+23_343+24del ENSP00000365402.5:n.343+23_343+24del
ENST00000376237.8:c.343+23_343+24del ENSP00000365412.4:n.343+23_343+24del
ENST00000383329.7:c.343+23_343+24del ENSP00000372819.3:n.343+23_343+24del
ENST00000415537.1:c.341+23_341+24del
ENST00000484378.1:n.385_386del
ENST00000487245.5:n.475_476del
ENST00000495835.1:n.532+23_532+24del
NM_002117.5:c.343+23_343+24del NP_002108.4:n.343+23_343+24del
NM_002117.6:c.343+23_343+24del MANE Select NP_002108.4:n.343+23_343+24del