Canonical Allele Identifier: CA2677949772

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269474-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269477del , CM000668.2:g.31269477del	GRCh38
NC_000006.11:g.31237254del , CM000668.1:g.31237254del	GRCh37
NC_000006.10:g.31345233del	NCBI36
NG_029422.2:g.7657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+18del MANE Select	ENSP00000365402.5:n.1048+18del
ENST00000376228.9:c.1048+18del	ENSP00000365402.5:n.1048+18del
ENST00000376237.8:c.*635+18del	ENSP00000365412.4:n.*635+18del
ENST00000383329.7:c.1066+18del	ENSP00000372819.3:n.1066+18del
ENST00000466892.5:n.192del
ENST00000470363.5:n.806+18del
ENST00000487245.5:n.1407+18del
NM_002117.5:c.1048+18del	NP_002108.4:n.1048+18del
NM_002117.6:c.1048+18del MANE Select	NP_002108.4:n.1048+18del