Canonical Allele Identifier: CA1619080775
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271658_31271660delinsGCC , CM000668.2:g.31271658_31271660delinsGCC GRCh38
NC_000006.11:g.31239435_31239437delinsGCC , CM000668.1:g.31239435_31239437delinsGCC GRCh37
NC_000006.10:g.31347414_31347416delinsGCC NCBI36
NG_029422.2:g.5472_5474delinsGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.282_284delinsGGC MANE Select ENSP00000365402.5:p.Gln94=
ENST00000376228.9:c.282_284delinsGGC ENSP00000365402.5:p.Gln94=
ENST00000376237.8:c.282_284delinsGGC ENSP00000365412.4:p.Gln94=
ENST00000383329.7:c.282_284delinsGGC ENSP00000372819.3:p.Gln94=
ENST00000415537.1:c.280_282delinsGGC
ENST00000484378.1:n.301_303delinsGGC
ENST00000487245.5:n.391_393delinsGGC
ENST00000495835.1:n.471_473delinsGGC
NM_002117.5:c.282_284delinsGGC NP_002108.4:p.Gln94=
NM_002117.6:c.282_284delinsGGC MANE Select NP_002108.4:p.Gln94=