Canonical Allele Identifier: CA2770491539
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271337_31271339delinsTGA , CM000668.2:g.31271337_31271339delinsTGA GRCh38
NC_000006.11:g.31239114_31239116delinsTGA , CM000668.1:g.31239114_31239116delinsTGA GRCh37
NC_000006.10:g.31347093_31347095delinsTGA NCBI36
NG_029422.2:g.5793_5795delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.353_355delinsTCA MANE Select ENSP00000365402.5:p.Thr118_Leu119delinsIleIle
ENST00000376228.9:c.353_355delinsTCA ENSP00000365402.5:p.Thr118_Leu119delinsIleIle
ENST00000376237.8:c.344-8_344-6delinsTCA ENSP00000365412.4:n.344-8_344-6delinsTCA
ENST00000383329.7:c.353_355delinsTCA ENSP00000372819.3:p.Thr118_Leu119delinsIleIle
ENST00000415537.1:c.351_353delinsTCA
ENST00000484378.1:n.622_624delinsTCA
ENST00000487245.5:n.712_714delinsTCA
ENST00000495835.1:n.542_544delinsTCA
NM_002117.5:c.353_355delinsTCA NP_002108.4:p.Thr118_Leu119delinsIleIle
NM_002117.6:c.353_355delinsTCA MANE Select NP_002108.4:p.Thr118_Leu119delinsIleIle
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