Canonical Allele Identifier: CA1619079946
Gene: HLA-C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270453_31270457delinsGGGGG , CM000668.2:g.31270453_31270457delinsGGGGG GRCh38
NC_000006.11:g.31238230_31238234delinsGGGGG , CM000668.1:g.31238230_31238234delinsGGGGG GRCh37
NC_000006.10:g.31346209_31346213delinsGGGGG NCBI36
NG_029422.2:g.6675_6679delinsCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.648_652delinsCCCCC MANE Select ENSP00000365402.5:p.His216=
ENST00000376228.9:c.648_652delinsCCCCC ENSP00000365402.5:p.His216=
ENST00000376237.8:c.*235_*239delinsCCCCC ENSP00000365412.4:n.*235_*239delinsCCCCC
ENST00000383329.7:c.648_652delinsCCCCC ENSP00000372819.3:p.His216=
ENST00000415537.1:c.646_650delinsCCCCC
ENST00000487245.5:n.1007_1011delinsCCCCC
ENST00000495835.1:n.837_841delinsCCCCC
NM_002117.5:c.648_652delinsCCCCC NP_002108.4:p.His216=
NM_002117.6:c.648_652delinsCCCCC MANE Select NP_002108.4:p.His216=
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