Canonical Allele Identifier: CA1619080333
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271126_31271135delinsACGCACGTGC , CM000668.2:g.31271126_31271135delinsACGCACGTGC GRCh38
NC_000006.11:g.31238903_31238912delinsACGCACGTGC , CM000668.1:g.31238903_31238912delinsACGCACGTGC GRCh37
NC_000006.10:g.31346882_31346891delinsACGCACGTGC NCBI36
NG_029422.2:g.5997_6006delinsGCACGTGCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.557_566delinsGCACGTGCGT MANE Select ENSP00000365402.5:p.Gly186=
ENST00000376228.9:c.557_566delinsGCACGTGCGT ENSP00000365402.5:p.Gly186=
ENST00000376237.8:c.*144_*153delinsGCACGTGCGT ENSP00000365412.4:n.*144_*153delinsGCACGTGCGT
ENST00000383329.7:c.557_566delinsGCACGTGCGT ENSP00000372819.3:p.Gly186=
ENST00000415537.1:c.555_564delinsGCACGTGCGT
ENST00000484378.1:n.826_835delinsGCACGTGCGT
ENST00000487245.5:n.916_925delinsGCACGTGCGT
ENST00000495835.1:n.746_755delinsGCACGTGCGT
NM_002117.5:c.557_566delinsGCACGTGCGT NP_002108.4:p.Gly186=
NM_002117.6:c.557_566delinsGCACGTGCGT MANE Select NP_002108.4:p.Gly186=