Canonical Allele Identifier: CA136866467

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860528
• MyVariant Identifiers: chr6:g.31238899_31238904del (hg19) ; chr6:g.31271122_31271127del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271122_31271127del , CM000668.2:g.31271122_31271127del	GRCh38
NC_000006.11:g.31238899_31238904del , CM000668.1:g.31238899_31238904del	GRCh37
NC_000006.10:g.31346878_31346883del	NCBI36
NG_029422.2:g.6005_6010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.565_570del MANE Select	ENSP00000365402.5:p.Val189_Glu190del
ENST00000376228.9:c.565_570del	ENSP00000365402.5:p.Val189_Glu190del
ENST00000376237.8:c.*152_*157del	ENSP00000365412.4:n.*152_*157del
ENST00000383329.7:c.565_570del	ENSP00000372819.3:p.Val189_Glu190del
ENST00000415537.1:c.563_568del
ENST00000484378.1:n.834_839del
ENST00000487245.5:n.924_929del
ENST00000495835.1:n.754_759del
NM_002117.5:c.565_570del	NP_002108.4:p.Val189_Glu190del
NM_002117.6:c.565_570del MANE Select	NP_002108.4:p.Val189_Glu190del