Canonical Allele Identifier: CA1087426153
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271044-T-TCA
gnomAD v4: 6-31271044-T-TCA
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271044_31271045insCA , CM000668.2:g.31271044_31271045insCA GRCh38
NC_000006.11:g.31238821_31238822insCA , CM000668.1:g.31238821_31238822insCA GRCh37
NC_000006.10:g.31346800_31346801insCA NCBI36
NG_029422.2:g.6087_6088insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+28_619+29insTG MANE Select ENSP00000365402.5:n.619+28_619+29insTG
ENST00000376228.9:c.619+28_619+29insTG ENSP00000365402.5:n.619+28_619+29insTG
ENST00000376237.8:c.*206+28_*206+29insTG ENSP00000365412.4:n.*206+28_*206+29insTG
ENST00000383329.7:c.619+28_619+29insTG ENSP00000372819.3:n.619+28_619+29insTG
ENST00000415537.1:c.617+28_617+29insTG
ENST00000487245.5:n.978+28_978+29insTG
ENST00000495835.1:n.808+28_808+29insTG
NM_002117.5:c.619+28_619+29insTG NP_002108.4:n.619+28_619+29insTG
NM_002117.6:c.619+28_619+29insTG MANE Select NP_002108.4:n.619+28_619+29insTG
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