Canonical Allele Identifier: CA1619080549

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761333807

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271346_31271347del , CM000668.2:g.31271346_31271347del	GRCh38
NC_000006.11:g.31239123_31239124del , CM000668.1:g.31239123_31239124del	GRCh37
NC_000006.10:g.31347102_31347103del	NCBI36
NG_029422.2:g.5785_5786del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.345_346del MANE Select	ENSP00000365402.5:p.Thr118ProfsTer20
ENST00000376228.9:c.345_346del	ENSP00000365402.5:p.Thr118ProfsTer20
ENST00000376237.8:c.344-16_344-15del	ENSP00000365412.4:n.344-16_344-15del
ENST00000383329.7:c.345_346del	ENSP00000372819.3:p.Thr118ProfsTer20
ENST00000415537.1:c.343_344del
ENST00000484378.1:n.614_615del
ENST00000487245.5:n.704_705del
ENST00000495835.1:n.534_535del
NM_002117.5:c.345_346del	NP_002108.4:p.Thr118ProfsTer20
NM_002117.6:c.345_346del MANE Select	NP_002108.4:p.Thr118ProfsTer20