Canonical Allele Identifier: CA2646987754

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737119del , CM000663.2:g.109737119del GRCh38
NC_000001.10:g.110279741del , CM000663.1:g.110279741del GRCh37
NC_000001.9:g.110081264del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.630del (GSTM3) MANE Select ENSP00000354357.2:p.Met210IlefsTer?
ENST00000256594.7:c.630del (GSTM3) ENSP00000256594.3:p.Met210IlefsTer?
ENST00000361066.6:c.630del (GSTM3) ENSP00000354357.2:p.Met210IlefsTer?
ENST00000429410.2:n.82+24771del (GSTM5)
ENST00000476321.5:n.598del (GSTM3)
ENST00000486823.5:n.594del (GSTM3)
ENST00000488824.1:n.975del (GSTM3)
NM_000849.4:c.630del (GSTM3) NP_000840.2:p.Met210IlefsTer?
NR_024537.1:n.864del (GSTM3)
XM_011541296.1:c.849del (GSTM3) XP_011539598.1:p.Met283IlefsTer?
NM_000849.5:c.630del (GSTM3) MANE Select NP_000840.2:p.Met210IlefsTer?
NR_024537.2:n.864del (GSTM3)