Canonical Allele Identifier: CA2677949675

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269397-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269397_31269398insG , CM000668.2:g.31269397_31269398insG	GRCh38
NC_000006.11:g.31237174_31237175insG , CM000668.1:g.31237174_31237175insG	GRCh37
NC_000006.10:g.31345153_31345154insG	NCBI36
NG_029422.2:g.7734_7735insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-13_1049-12insC MANE Select	ENSP00000365402.5:n.1049-13_1049-12insC
ENST00000376228.9:c.1049-13_1049-12insC	ENSP00000365402.5:n.1049-13_1049-12insC
ENST00000376237.8:c.*636-13_*636-12insC	ENSP00000365412.4:n.*636-13_*636-12insC
ENST00000383329.7:c.1067-13_1067-12insC	ENSP00000372819.3:n.1067-13_1067-12insC
ENST00000466892.5:n.269_270insC
ENST00000470363.5:n.807-13_807-12insC
ENST00000487245.5:n.1408-13_1408-12insC
NM_002117.5:c.1049-13_1049-12insC	NP_002108.4:n.1049-13_1049-12insC
NM_002117.6:c.1049-13_1049-12insC MANE Select	NP_002108.4:n.1049-13_1049-12insC