Canonical Allele Identifier: CA2677949750

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269455-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269456_31269457del , CM000668.2:g.31269456_31269457del	GRCh38
NC_000006.11:g.31237233_31237234del , CM000668.1:g.31237233_31237234del	GRCh37
NC_000006.10:g.31345212_31345213del	NCBI36
NG_029422.2:g.7675_7676del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+36_1048+37del MANE Select	ENSP00000365402.5:n.1048+36_1048+37del
ENST00000376228.9:c.1048+36_1048+37del	ENSP00000365402.5:n.1048+36_1048+37del
ENST00000376237.8:c.*635+36_*635+37del	ENSP00000365412.4:n.*635+36_*635+37del
ENST00000383329.7:c.1066+36_1066+37del	ENSP00000372819.3:n.1066+36_1066+37del
ENST00000466892.5:n.210_211del
ENST00000470363.5:n.806+36_806+37del
ENST00000487245.5:n.1407+36_1407+37del
NM_002117.5:c.1048+36_1048+37del	NP_002108.4:n.1048+36_1048+37del
NM_002117.6:c.1048+36_1048+37del MANE Select	NP_002108.4:n.1048+36_1048+37del