Canonical Allele Identifier: CA2646988082

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737319_109737320del , CM000663.2:g.109737319_109737320del GRCh38
NC_000001.10:g.110279941_110279942del , CM000663.1:g.110279941_110279942del GRCh37
NC_000001.9:g.110081464_110081465del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.579+137_579+138del (GSTM3) MANE Select ENSP00000354357.2:n.579+137_579+138del
ENST00000256594.7:c.579+137_579+138del (GSTM3) ENSP00000256594.3:n.579+137_579+138del
ENST00000361066.6:c.579+137_579+138del (GSTM3) ENSP00000354357.2:n.579+137_579+138del
ENST00000429410.2:n.82+24971_82+24972del (GSTM5)
ENST00000476321.5:n.397_398del (GSTM3)
ENST00000486823.5:n.543+137_543+138del (GSTM3)
ENST00000488824.1:n.924+137_924+138del (GSTM3)
NM_000849.4:c.579+137_579+138del (GSTM3) NP_000840.2:n.579+137_579+138del
NR_024537.1:n.813+137_813+138del (GSTM3)
XM_011541296.1:c.798+137_798+138del (GSTM3) XP_011539598.1:n.798+137_798+138del
NM_000849.5:c.579+137_579+138del (GSTM3) MANE Select NP_000840.2:n.579+137_579+138del
NR_024537.2:n.813+137_813+138del (GSTM3)