Canonical Allele Identifier: CA2677951270

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271150-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271151_31271152insTT , CM000668.2:g.31271151_31271152insTT	GRCh38
NC_000006.11:g.31238928_31238929insTT , CM000668.1:g.31238928_31238929insTT	GRCh37
NC_000006.10:g.31346907_31346908insTT	NCBI36
NG_029422.2:g.5981_5982insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.541_542insAA MANE Select	ENSP00000365402.5:p.Arg181LysfsTer?
ENST00000376228.9:c.541_542insAA	ENSP00000365402.5:p.Arg181LysfsTer?
ENST00000376237.8:c.*128_*129insAA	ENSP00000365412.4:n.*128_*129insAA
ENST00000383329.7:c.541_542insAA	ENSP00000372819.3:p.Arg181LysfsTer?
ENST00000415537.1:c.539_540insAA
ENST00000484378.1:n.810_811insAA
ENST00000487245.5:n.900_901insAA
ENST00000495835.1:n.730_731insAA
NM_002117.5:c.541_542insAA	NP_002108.4:p.Arg181LysfsTer?
NM_002117.6:c.541_542insAA MANE Select	NP_002108.4:p.Arg181LysfsTer?