Canonical Allele Identifier: CA1188220528

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737265_109737266delinsTC , CM000663.2:g.109737265_109737266delinsTC GRCh38
NC_000001.10:g.110279887_110279888delinsTC , CM000663.1:g.110279887_110279888delinsTC GRCh37
NC_000001.9:g.110081410_110081411delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-97_580-96delinsGA (GSTM3) MANE Select ENSP00000354357.2:n.580-97_580-96delinsGA
ENST00000256594.7:c.580-97_580-96delinsGA (GSTM3) ENSP00000256594.3:n.580-97_580-96delinsGA
ENST00000361066.6:c.580-97_580-96delinsGA (GSTM3) ENSP00000354357.2:n.580-97_580-96delinsGA
ENST00000429410.2:n.82+24917_82+24918delinsTC (GSTM5)
ENST00000476321.5:n.451_452delinsGA (GSTM3)
ENST00000486823.5:n.544-97_544-96delinsGA (GSTM3)
ENST00000488824.1:n.925-97_925-96delinsGA (GSTM3)
NM_000849.4:c.580-97_580-96delinsGA (GSTM3) NP_000840.2:n.580-97_580-96delinsGA
NR_024537.1:n.814-97_814-96delinsGA (GSTM3)
XM_011541296.1:c.799-97_799-96delinsGA (GSTM3) XP_011539598.1:n.799-97_799-96delinsGA
NM_000849.5:c.580-97_580-96delinsGA (GSTM3) MANE Select NP_000840.2:n.580-97_580-96delinsGA
NR_024537.2:n.814-97_814-96delinsGA (GSTM3)