Canonical Allele Identifier: CA2711332856
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2113902601
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269500_31269501insA , CM000668.2:g.31269500_31269501insA GRCh38
NC_000006.11:g.31237277_31237278insA , CM000668.1:g.31237277_31237278insA GRCh37
NC_000006.10:g.31345256_31345257insA NCBI36
NG_029422.2:g.7631_7632insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1040_1041insT MANE Select ENSP00000365402.5:p.Gln347HisfsTer12
ENST00000376228.9:c.1040_1041insT ENSP00000365402.5:p.Gln347HisfsTer12
ENST00000376237.8:c.*627_*628insT ENSP00000365412.4:n.*627_*628insT
ENST00000383329.7:c.1058_1059insT ENSP00000372819.3:p.Gln353HisfsTer12
ENST00000466892.5:n.166_167insT
ENST00000470363.5:n.798_799insT
ENST00000487245.5:n.1399_1400insT
NM_002117.5:c.1040_1041insT NP_002108.4:p.Gln347HisfsTer12
NM_002117.6:c.1040_1041insT MANE Select NP_002108.4:p.Gln347HisfsTer12
Search 100 bp 5'
Search 100 bp 3'