Canonical Allele Identifier: CA823863407
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1392634751

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271337_31271339del , CM000668.2:g.31271337_31271339del GRCh38
NC_000006.11:g.31239114_31239116del , CM000668.1:g.31239114_31239116del GRCh37
NC_000006.10:g.31347093_31347095del NCBI36
NG_029422.2:g.5793_5795del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.353_355del MANE Select ENSP00000365402.5:p.Thr118_Leu119delinsIl...
ENST00000376228.9:c.353_355del ENSP00000365402.5:p.Thr118_Leu119delinsIl...
ENST00000376237.8:c.344-8_344-6del ENSP00000365412.4:n.344-8_344-6del
ENST00000383329.7:c.353_355del ENSP00000372819.3:p.Thr118_Leu119delinsIl...
ENST00000415537.1:c.351_353del
ENST00000484378.1:n.622_624del
ENST00000487245.5:n.712_714del
ENST00000495835.1:n.542_544del
NM_002117.5:c.353_355del NP_002108.4:p.Thr118_Leu119delinsIle
NM_002117.6:c.353_355del MANE Select NP_002108.4:p.Thr118_Leu119delinsIle