Canonical Allele Identifier: CA525627041

Linked Data

dbSNP Id: rs1557979133

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737379del , CM000663.2:g.109737379del GRCh38
NC_000001.10:g.110280001del , CM000663.1:g.110280001del GRCh37
NC_000001.9:g.110081524del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.579+79del (GSTM3) MANE Select ENSP00000354357.2:n.579+79del
ENST00000256594.7:c.579+79del (GSTM3) ENSP00000256594.3:n.579+79del
ENST00000361066.6:c.579+79del (GSTM3) ENSP00000354357.2:n.579+79del
ENST00000429410.2:n.82+25031del (GSTM5)
ENST00000476321.5:n.339del (GSTM3)
ENST00000486823.5:n.543+79del (GSTM3)
ENST00000488824.1:n.924+79del (GSTM3)
ENST00000540225.2:c.*9del (GSTM3) ENSP00000444978.2:n.*9del
NM_000849.4:c.579+79del (GSTM3) NP_000840.2:n.579+79del
NR_024537.1:n.813+79del (GSTM3)
XM_011541296.1:c.798+79del (GSTM3) XP_011539598.1:n.798+79del
NM_000849.5:c.579+79del (GSTM3) MANE Select NP_000840.2:n.579+79del
NR_024537.2:n.813+79del (GSTM3)