Canonical Allele Identifier: CA1619080282
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271073_31271074delinsCT , CM000668.2:g.31271073_31271074delinsCT GRCh38
NC_000006.11:g.31238850_31238851delinsCT , CM000668.1:g.31238850_31238851delinsCT GRCh37
NC_000006.10:g.31346829_31346830delinsCT NCBI36
NG_029422.2:g.6058_6059delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.618_619delinsAG MANE Select ENSP00000365402.5:p.Ala206=
ENST00000376228.9:c.618_619delinsAG ENSP00000365402.5:p.Ala206=
ENST00000376237.8:c.*205_*206delinsAG ENSP00000365412.4:n.*205_*206delinsAG
ENST00000383329.7:c.618_619delinsAG ENSP00000372819.3:p.Ala206=
ENST00000415537.1:c.616_617delinsAG
ENST00000487245.5:n.977_978delinsAG
ENST00000495835.1:n.807_808delinsAG
NM_002117.5:c.618_619delinsAG NP_002108.4:p.Ala206=
NM_002117.6:c.618_619delinsAG MANE Select NP_002108.4:p.Ala206=