Canonical Allele Identifier: CA2677950478

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270114-CTGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270115_31270117del , CM000668.2:g.31270115_31270117del	GRCh38
NC_000006.11:g.31237892_31237894del , CM000668.1:g.31237892_31237894del	GRCh37
NC_000006.10:g.31345871_31345873del	NCBI36
NG_029422.2:g.7015_7017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.896-32_896-30del MANE Select	ENSP00000365402.5:n.896-32_896-30del
ENST00000376228.9:c.896-32_896-30del	ENSP00000365402.5:n.896-32_896-30del
ENST00000376237.8:c.*483-32_*483-30del	ENSP00000365412.4:n.*483-32_*483-30del
ENST00000383329.7:c.896-32_896-30del	ENSP00000372819.3:n.896-32_896-30del
ENST00000470363.5:n.214-32_214-30del
ENST00000487245.5:n.1255-32_1255-30del
NM_002117.5:c.896-32_896-30del	NP_002108.4:n.896-32_896-30del
NM_002117.6:c.896-32_896-30del MANE Select	NP_002108.4:n.896-32_896-30del