Canonical Allele Identifier: CA2677951714
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271658_31271659insTGTTGG , CM000668.2:g.31271658_31271659insTGTTGG GRCh38
NC_000006.11:g.31239435_31239436insTGTTGG , CM000668.1:g.31239435_31239436insTGTTGG GRCh37
NC_000006.10:g.31347414_31347415insTGTTGG NCBI36
NG_029422.2:g.5474_5475insCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.284_285insCAACAC MANE Select ENSP00000365402.5:p.Ala95_Gln96insAsnThr
ENST00000376228.9:c.284_285insCAACAC ENSP00000365402.5:p.Ala95_Gln96insAsnThr
ENST00000376237.8:c.284_285insCAACAC ENSP00000365412.4:p.Ala95_Gln96insAsnThr
ENST00000383329.7:c.284_285insCAACAC ENSP00000372819.3:p.Ala95_Gln96insAsnThr
ENST00000415537.1:c.282_283insCAACAC
ENST00000484378.1:n.303_304insCAACAC
ENST00000487245.5:n.393_394insCAACAC
ENST00000495835.1:n.473_474insCAACAC
NM_002117.5:c.284_285insCAACAC NP_002108.4:p.Ala95_Gln96insAsnThr
NM_002117.6:c.284_285insCAACAC MANE Select NP_002108.4:p.Ala95_Gln96insAsnThr