Canonical Allele Identifier: CA2677949099
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268906-C-CG
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268906_31268907insG , CM000668.2:g.31268906_31268907insG GRCh38
NC_000006.11:g.31236683_31236684insG , CM000668.1:g.31236683_31236684insG GRCh37
NC_000006.10:g.31344662_31344663insG NCBI36
NG_029422.2:g.8225_8226insC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*262_*263insC MANE Select ENSP00000365402.5:n.*262_*263insC
ENST00000376228.9:c.*262_*263insC ENSP00000365402.5:n.*262_*263insC
ENST00000376237.8:c.*950_*951insC ENSP00000365412.4:n.*950_*951insC
ENST00000383329.7:c.*262_*263insC ENSP00000372819.3:n.*262_*263insC
ENST00000466892.5:n.596_597insC
ENST00000470363.5:n.1121_1122insC
ENST00000487245.5:n.1722_1723insC
NM_002117.5:c.*262_*263insC NP_002108.4:n.*262_*263insC
NM_002117.6:c.*262_*263insC MANE Select NP_002108.4:n.*262_*263insC
Search 100 bp 5'
Search 100 bp 3'