Canonical Allele Identifier: CA2677951333
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271286_31271287insTGTCC , CM000668.2:g.31271286_31271287insTGTCC GRCh38
NC_000006.11:g.31239063_31239064insTGTCC , CM000668.1:g.31239063_31239064insTGTCC GRCh37
NC_000006.10:g.31347042_31347043insTGTCC NCBI36
NG_029422.2:g.5847_5848insACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.407_408insACAGG MANE Select ENSP00000365402.5:p.Tyr137GlnfsTer16
ENST00000376228.9:c.407_408insACAGG ENSP00000365402.5:p.Tyr137GlnfsTer16
ENST00000376237.8:c.390_391insACAGG ENSP00000365412.4:p.Val131ThrfsTer?
ENST00000383329.7:c.407_408insACAGG ENSP00000372819.3:p.Tyr137GlnfsTer16
ENST00000415537.1:c.405_406insACAGG
ENST00000484378.1:n.676_677insACAGG
ENST00000487245.5:n.766_767insACAGG
ENST00000495835.1:n.596_597insACAGG
NM_002117.5:c.407_408insACAGG NP_002108.4:p.Tyr137GlnfsTer16
NM_002117.6:c.407_408insACAGG MANE Select NP_002108.4:p.Tyr137GlnfsTer16