Canonical Allele Identifier: CA2677949667

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269392-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269394_31269395del , CM000668.2:g.31269394_31269395del	GRCh38
NC_000006.11:g.31237171_31237172del , CM000668.1:g.31237171_31237172del	GRCh37
NC_000006.10:g.31345150_31345151del	NCBI36
NG_029422.2:g.7738_7739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-9_1049-8del MANE Select	ENSP00000365402.5:n.1049-9_1049-8del
ENST00000376228.9:c.1049-9_1049-8del	ENSP00000365402.5:n.1049-9_1049-8del
ENST00000376237.8:c.*636-9_*636-8del	ENSP00000365412.4:n.*636-9_*636-8del
ENST00000383329.7:c.1067-9_1067-8del	ENSP00000372819.3:n.1067-9_1067-8del
ENST00000466892.5:n.273_274del
ENST00000470363.5:n.807-9_807-8del
ENST00000487245.5:n.1408-9_1408-8del
NM_002117.5:c.1049-9_1049-8del	NP_002108.4:n.1049-9_1049-8del
NM_002117.6:c.1049-9_1049-8del MANE Select	NP_002108.4:n.1049-9_1049-8del