Canonical Allele Identifier: CA2677949779

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269480-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269481dup , CM000668.2:g.31269481dup	GRCh38
NC_000006.11:g.31237258dup , CM000668.1:g.31237258dup	GRCh37
NC_000006.10:g.31345237dup	NCBI36
NG_029422.2:g.7651dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+12dup MANE Select	ENSP00000365402.5:n.1048+12dup
ENST00000376228.9:c.1048+12dup	ENSP00000365402.5:n.1048+12dup
ENST00000376237.8:c.*635+12dup	ENSP00000365412.4:n.*635+12dup
ENST00000383329.7:c.1066+12dup	ENSP00000372819.3:n.1066+12dup
ENST00000466892.5:n.186dup
ENST00000470363.5:n.806+12dup
ENST00000487245.5:n.1407+12dup
NM_002117.5:c.1048+12dup	NP_002108.4:n.1048+12dup
NM_002117.6:c.1048+12dup MANE Select	NP_002108.4:n.1048+12dup