Canonical Allele Identifier: CA1188220341

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736750_109736751delinsAG , CM000663.2:g.109736750_109736751delinsAG GRCh38
NC_000001.10:g.110279372_110279373delinsAG , CM000663.1:g.110279372_110279373delinsAG GRCh37
NC_000001.9:g.110080895_110080896delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*320_*321delinsCT (GSTM3) MANE Select ENSP00000354357.2:n.*320_*321delinsCT
ENST00000256594.7:c.*320_*321delinsCT (GSTM3) ENSP00000256594.3:n.*320_*321delinsCT
ENST00000361066.6:c.*320_*321delinsCT (GSTM3) ENSP00000354357.2:n.*320_*321delinsCT
ENST00000429410.2:n.82+24402_82+24403delinsAG (GSTM5)
NM_000849.4:c.*320_*321delinsCT (GSTM3) NP_000840.2:n.*320_*321delinsCT
NR_024537.1:n.1232_1233delinsCT (GSTM3)
NM_000849.5:c.*320_*321delinsCT (GSTM3) MANE Select NP_000840.2:n.*320_*321delinsCT
NR_024537.2:n.1232_1233delinsCT (GSTM3)