Canonical Allele Identifier: CA1188220444

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737076_109737079delinsATAC , CM000663.2:g.109737076_109737079delinsATAC GRCh38
NC_000001.10:g.110279698_110279701delinsATAC , CM000663.1:g.110279698_110279701delinsATAC GRCh37
NC_000001.9:g.110081221_110081224delinsATAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.670_673delinsGTAT (GSTM3) MANE Select ENSP00000354357.2:p.Val224=
ENST00000256594.7:c.670_673delinsGTAT (GSTM3) ENSP00000256594.3:p.Val224=
ENST00000361066.6:c.670_673delinsGTAT (GSTM3) ENSP00000354357.2:p.Val224=
ENST00000429410.2:n.82+24728_82+24731delinsATAC (GSTM5)
ENST00000476321.5:n.638_641delinsGTAT (GSTM3)
ENST00000486823.5:n.634_637delinsGTAT (GSTM3)
ENST00000488824.1:n.1015_1018delinsGTAT (GSTM3)
NM_000849.4:c.670_673delinsGTAT (GSTM3) NP_000840.2:p.Val224=
NR_024537.1:n.904_907delinsGTAT (GSTM3)
XM_011541296.1:c.889_892delinsGTAT (GSTM3) XP_011539598.1:p.Val297=
NM_000849.5:c.670_673delinsGTAT (GSTM3) MANE Select NP_000840.2:p.Val224=
NR_024537.2:n.904_907delinsGTAT (GSTM3)