Canonical Allele Identifier: CA2677951239

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271122-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271122_31271123insG , CM000668.2:g.31271122_31271123insG	GRCh38
NC_000006.11:g.31238899_31238900insG , CM000668.1:g.31238899_31238900insG	GRCh37
NC_000006.10:g.31346878_31346879insG	NCBI36
NG_029422.2:g.6009_6010insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.569_570insC MANE Select	ENSP00000365402.5:p.Glu190AspfsTer31
ENST00000376228.9:c.569_570insC	ENSP00000365402.5:p.Glu190AspfsTer31
ENST00000376237.8:c.*156_*157insC	ENSP00000365412.4:n.*156_*157insC
ENST00000383329.7:c.569_570insC	ENSP00000372819.3:p.Glu190AspfsTer31
ENST00000415537.1:c.567_568insC
ENST00000484378.1:n.838_839insC
ENST00000487245.5:n.928_929insC
ENST00000495835.1:n.758_759insC
NM_002117.5:c.569_570insC	NP_002108.4:p.Glu190AspfsTer31
NM_002117.6:c.569_570insC MANE Select	NP_002108.4:p.Glu190AspfsTer31