Canonical Allele Identifier: CA1188220512

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737237_109737238delinsCA , CM000663.2:g.109737237_109737238delinsCA GRCh38
NC_000001.10:g.110279859_110279860delinsCA , CM000663.1:g.110279859_110279860delinsCA GRCh37
NC_000001.9:g.110081382_110081383delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-69_580-68delinsTG (GSTM3) MANE Select ENSP00000354357.2:n.580-69_580-68delinsTG
ENST00000256594.7:c.580-69_580-68delinsTG (GSTM3) ENSP00000256594.3:n.580-69_580-68delinsTG
ENST00000361066.6:c.580-69_580-68delinsTG (GSTM3) ENSP00000354357.2:n.580-69_580-68delinsTG
ENST00000429410.2:n.82+24889_82+24890delinsCA (GSTM5)
ENST00000476321.5:n.479_480delinsTG (GSTM3)
ENST00000486823.5:n.544-69_544-68delinsTG (GSTM3)
ENST00000488824.1:n.925-69_925-68delinsTG (GSTM3)
NM_000849.4:c.580-69_580-68delinsTG (GSTM3) NP_000840.2:n.580-69_580-68delinsTG
NR_024537.1:n.814-69_814-68delinsTG (GSTM3)
XM_011541296.1:c.799-69_799-68delinsTG (GSTM3) XP_011539598.1:n.799-69_799-68delinsTG
NM_000849.5:c.580-69_580-68delinsTG (GSTM3) MANE Select NP_000840.2:n.580-69_580-68delinsTG
NR_024537.2:n.814-69_814-68delinsTG (GSTM3)