Canonical Allele Identifier: CA3710849
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs773033113

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271563_31271565del , CM000668.2:g.31271563_31271565del GRCh38
NC_000006.11:g.31239340_31239342del , CM000668.1:g.31239340_31239342del GRCh37
NC_000006.10:g.31347319_31347321del NCBI36
NG_029422.2:g.5568_5570del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+35_343+37del MANE Select ENSP00000365402.5:n.343+35_343+37del
ENST00000376228.9:c.343+35_343+37del ENSP00000365402.5:n.343+35_343+37del
ENST00000376237.8:c.343+35_343+37del ENSP00000365412.4:n.343+35_343+37del
ENST00000383329.7:c.343+35_343+37del ENSP00000372819.3:n.343+35_343+37del
ENST00000415537.1:c.341+35_341+37del
ENST00000484378.1:n.397_399del
ENST00000487245.5:n.487_489del
ENST00000495835.1:n.532+35_532+37del
NM_002117.5:c.343+35_343+37del NP_002108.4:n.343+35_343+37del
NM_002117.6:c.343+35_343+37del MANE Select NP_002108.4:n.343+35_343+37del