Canonical Allele Identifier: CA2677950491

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270118-CCCCCAAGCCTCAGCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270119_31270135del , CM000668.2:g.31270119_31270135del	GRCh38
NC_000006.11:g.31237896_31237912del , CM000668.1:g.31237896_31237912del	GRCh37
NC_000006.10:g.31345875_31345891del	NCBI36
NG_029422.2:g.6997_7013del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.896-50_896-34del MANE Select	ENSP00000365402.5:n.896-50_896-34del
ENST00000376228.9:c.896-50_896-34del	ENSP00000365402.5:n.896-50_896-34del
ENST00000376237.8:c.*483-50_*483-34del	ENSP00000365412.4:n.*483-50_*483-34del
ENST00000383329.7:c.896-50_896-34del	ENSP00000372819.3:n.896-50_896-34del
ENST00000470363.5:n.214-50_214-34del
ENST00000487245.5:n.1255-50_1255-34del
NM_002117.5:c.896-50_896-34del	NP_002108.4:n.896-50_896-34del
NM_002117.6:c.896-50_896-34del MANE Select	NP_002108.4:n.896-50_896-34del