Canonical Allele Identifier: CA1619080344
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271133_31271135delinsTGC , CM000668.2:g.31271133_31271135delinsTGC GRCh38
NC_000006.11:g.31238910_31238912delinsTGC , CM000668.1:g.31238910_31238912delinsTGC GRCh37
NC_000006.10:g.31346889_31346891delinsTGC NCBI36
NG_029422.2:g.5997_5999delinsGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.557_559delinsGCA MANE Select ENSP00000365402.5:p.Gly186=
ENST00000376228.9:c.557_559delinsGCA ENSP00000365402.5:p.Gly186=
ENST00000376237.8:c.*144_*146delinsGCA ENSP00000365412.4:n.*144_*146delinsGCA
ENST00000383329.7:c.557_559delinsGCA ENSP00000372819.3:p.Gly186=
ENST00000415537.1:c.555_557delinsGCA
ENST00000484378.1:n.826_828delinsGCA
ENST00000487245.5:n.916_918delinsGCA
ENST00000495835.1:n.746_748delinsGCA
NM_002117.5:c.557_559delinsGCA NP_002108.4:p.Gly186=
NM_002117.6:c.557_559delinsGCA MANE Select NP_002108.4:p.Gly186=