Canonical Allele Identifier: CA3047149228
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271323_31271324delinsGT , CM000668.2:g.31271323_31271324delinsGT GRCh38
NC_000006.11:g.31239100_31239101delinsGT , CM000668.1:g.31239100_31239101delinsGT GRCh37
NC_000006.10:g.31347079_31347080delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.368_369delinsAC MANE Select ENSP00000365402.5:p.Ser123Tyr
ENST00000376228.9:c.368_369delinsAC ENSP00000365402.5:p.Ser123Tyr
ENST00000376237.8:c.351_352delinsAC ENSP00000365412.4:p.Trp118Arg
ENST00000383329.7:c.368_369delinsAC ENSP00000372819.3:p.Ser123Tyr
ENST00000415537.1:c.366_367delinsAC
ENST00000484378.1:n.637_638delinsAC
ENST00000487245.5:n.727_728delinsAC
ENST00000495835.1:n.557_558delinsAC
NM_002117.5:c.368_369delinsAC NP_002108.4:p.Ser123Tyr
NM_002117.6:c.368_369delinsAC MANE Select NP_002108.4:p.Ser123Tyr