Canonical Allele Identifier: CA2677951207
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271073-CTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271074_31271075del , CM000668.2:g.31271074_31271075del GRCh38
NC_000006.11:g.31238851_31238852del , CM000668.1:g.31238851_31238852del GRCh37
NC_000006.10:g.31346830_31346831del NCBI36
NG_029422.2:g.6057_6058del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.617_618del MANE Select ENSP00000365402.5:p.Ala206GlyfsTer14
ENST00000376228.9:c.617_618del ENSP00000365402.5:p.Ala206GlyfsTer14
ENST00000376237.8:c.*204_*205del ENSP00000365412.4:n.*204_*205del
ENST00000383329.7:c.617_618del ENSP00000372819.3:p.Ala206GlyfsTer14
ENST00000415537.1:c.615_616del
ENST00000487245.5:n.976_977del
ENST00000495835.1:n.806_807del
NM_002117.5:c.617_618del NP_002108.4:p.Ala206GlyfsTer14
NM_002117.6:c.617_618del MANE Select NP_002108.4:p.Ala206GlyfsTer14
Search 100 bp 5'
Search 100 bp 3'