Canonical Allele Identifier: CA2677951250

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271133-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271133_31271134insC , CM000668.2:g.31271133_31271134insC	GRCh38
NC_000006.11:g.31238910_31238911insC , CM000668.1:g.31238910_31238911insC	GRCh37
NC_000006.10:g.31346889_31346890insC	NCBI36
NG_029422.2:g.5998_5999insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.558_559insG MANE Select	ENSP00000365402.5:p.Thr187AspfsTer?
ENST00000376228.9:c.558_559insG	ENSP00000365402.5:p.Thr187AspfsTer?
ENST00000376237.8:c.*145_*146insG	ENSP00000365412.4:n.*145_*146insG
ENST00000383329.7:c.558_559insG	ENSP00000372819.3:p.Thr187AspfsTer?
ENST00000415537.1:c.556_557insG
ENST00000484378.1:n.827_828insG
ENST00000487245.5:n.917_918insG
ENST00000495835.1:n.747_748insG
NM_002117.5:c.558_559insG	NP_002108.4:p.Thr187AspfsTer?
NM_002117.6:c.558_559insG MANE Select	NP_002108.4:p.Thr187AspfsTer?