Canonical Allele Identifier: CA3710702

Gene: HLA-C

Linked Data

• dbSNP Id: rs779505818
• ExAC: 6:31238931 G / GTC
• gnomAD v2: 6-31238931-G-GTC
• gnomAD v3: 6-31271154-G-GTC
• gnomAD v4: 6-31271154-G-GTC
• MyVariant Identifiers: chr6:g.31238931_31238932insTC (hg19) ; chr6:g.31271154_31271155insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271154_31271155insTC , CM000668.2:g.31271154_31271155insTC	GRCh38
NC_000006.11:g.31238931_31238932insTC , CM000668.1:g.31238931_31238932insTC	GRCh37
NC_000006.10:g.31346910_31346911insTC	NCBI36
NG_029422.2:g.5977_5978insGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.537_538insGA MANE Select	ENSP00000365402.5:p.Leu180AspfsTer2
ENST00000376228.9:c.537_538insGA	ENSP00000365402.5:p.Leu180AspfsTer2
ENST00000376237.8:c.*124_*125insGA	ENSP00000365412.4:n.*124_*125insGA
ENST00000383329.7:c.537_538insGA	ENSP00000372819.3:p.Leu180AspfsTer2
ENST00000415537.1:c.535_536insGA
ENST00000484378.1:n.806_807insGA
ENST00000487245.5:n.896_897insGA
ENST00000495835.1:n.726_727insGA
NM_002117.5:c.537_538insGA	NP_002108.4:p.Leu180AspfsTer2
NM_002117.6:c.537_538insGA MANE Select	NP_002108.4:p.Leu180AspfsTer2