Canonical Allele Identifier: CA2677950297
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269999-C-CAGCCCT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269999_31270000insAGCCCT , CM000668.2:g.31269999_31270000insAGCCCT GRCh38
NC_000006.11:g.31237776_31237777insAGCCCT , CM000668.1:g.31237776_31237777insAGCCCT GRCh37
NC_000006.10:g.31345755_31345756insAGCCCT NCBI36
NG_029422.2:g.7132_7133insAGGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.981_982insAGGGCT MANE Select ENSP00000365402.5:p.Val327_Val328insArgAla
ENST00000376228.9:c.981_982insAGGGCT ENSP00000365402.5:p.Val327_Val328insArgAla
ENST00000376237.8:c.*568_*569insAGGGCT ENSP00000365412.4:n.*568_*569insAGGGCT
ENST00000383329.7:c.981_982insAGGGCT ENSP00000372819.3:p.Val327_Val328insArgAla
ENST00000470363.5:n.299_300insAGGGCT
ENST00000487245.5:n.1340_1341insAGGGCT
NM_002117.5:c.981_982insAGGGCT NP_002108.4:p.Val327_Val328insArgAla
NM_002117.6:c.981_982insAGGGCT MANE Select NP_002108.4:p.Val327_Val328insArgAla
Search 100 bp 5'
Search 100 bp 3'