Canonical Allele Identifier: CA2646987728

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737101del , CM000663.2:g.109737101del GRCh38
NC_000001.10:g.110279723del , CM000663.1:g.110279723del GRCh37
NC_000001.9:g.110081246del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.649del (GSTM3) MANE Select ENSP00000354357.2:p.Ala217ProfsTer?
ENST00000256594.7:c.649del (GSTM3) ENSP00000256594.3:p.Ala217ProfsTer?
ENST00000361066.6:c.649del (GSTM3) ENSP00000354357.2:p.Ala217ProfsTer?
ENST00000429410.2:n.82+24753del (GSTM5)
ENST00000476321.5:n.617del (GSTM3)
ENST00000486823.5:n.613del (GSTM3)
ENST00000488824.1:n.994del (GSTM3)
NM_000849.4:c.649del (GSTM3) NP_000840.2:p.Ala217ProfsTer?
NR_024537.1:n.883del (GSTM3)
XM_011541296.1:c.868del (GSTM3) XP_011539598.1:p.Ala290ProfsTer?
NM_000849.5:c.649del (GSTM3) MANE Select NP_000840.2:p.Ala217ProfsTer?
NR_024537.2:n.883del (GSTM3)