Canonical Allele Identifier: CA3710438

Gene: HLA-C

Linked Data

• dbSNP Id: rs781427080
• ExAC: 6:31237962 TGTGA / T
• gnomAD v4: 6-31270185-TGTGA-T
• MyVariant Identifiers: chr6:g.31237963_31237966del (hg19) ; chr6:g.31270186_31270189del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270186_31270189del , CM000668.2:g.31270186_31270189del	GRCh38
NC_000006.11:g.31237963_31237966del , CM000668.1:g.31237963_31237966del	GRCh37
NC_000006.10:g.31345942_31345945del	NCBI36
NG_029422.2:g.6943_6946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.895+21_895+24del MANE Select	ENSP00000365402.5:n.895+21_895+24del
ENST00000376228.9:c.895+21_895+24del	ENSP00000365402.5:n.895+21_895+24del
ENST00000376237.8:c.*482+21_*482+24del	ENSP00000365412.4:n.*482+21_*482+24del
ENST00000383329.7:c.895+21_895+24del	ENSP00000372819.3:n.895+21_895+24del
ENST00000470363.5:n.213+21_213+24del
ENST00000487245.5:n.1254+21_1254+24del
NM_002117.5:c.895+21_895+24del	NP_002108.4:n.895+21_895+24del
NM_002117.6:c.895+21_895+24del MANE Select	NP_002108.4:n.895+21_895+24del