Canonical Allele Identifier: CA2677951301
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271209_31271220del , CM000668.2:g.31271209_31271220del GRCh38
NC_000006.11:g.31238986_31238997del , CM000668.1:g.31238986_31238997del GRCh37
NC_000006.10:g.31346965_31346976del NCBI36
NG_029422.2:g.5917_5928del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.477_488del MANE Select ENSP00000365402.5:p.Ala160_Ala163del
ENST00000376228.9:c.477_488del ENSP00000365402.5:p.Ala160_Ala163del
ENST00000376237.8:c.*64_*75del ENSP00000365412.4:n.*64_*75del
ENST00000383329.7:c.477_488del ENSP00000372819.3:p.Ala160_Ala163del
ENST00000415537.1:c.475_486del
ENST00000484378.1:n.746_757del
ENST00000487245.5:n.836_847del
ENST00000495835.1:n.666_677del
NM_002117.5:c.477_488del NP_002108.4:p.Ala160_Ala163del
NM_002117.6:c.477_488del MANE Select NP_002108.4:p.Ala160_Ala163del