Canonical Allele Identifier: CA1139808456
Gene: GSTM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109657738T= , CM000663.2:g.109657738T= GRCh38
NC_000001.10:g.110200360T= , CM000663.1:g.110200360T= GRCh37
NC_000001.9:g.110001883T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000850.5:c.260-34T= MANE Select NP_000841.1:n.260-34T=
ENST00000369836.9:c.260-34T= MANE Select ENSP00000358851.4:n.260-34T=
NM_000850.4:c.260-34T= NP_000841.1:n.260-34T=
NM_147148.2:c.260-34T= NP_671489.1:n.260-34T=
NM_147148.3:c.260-34T= NP_671489.1:n.260-34T=
NR_024538.1:n.492-34T=
NR_024538.2:n.469-34T=
ENST00000326729.9:c.260-34T= ENSP00000316471.5:n.260-34T=
ENST00000336075.6:c.260-34T= ENSP00000336744.6:n.260-34T=
ENST00000369833.5:c.137-34T= ENSP00000358848.1:n.137-34T=
ENST00000369836.8:c.260-34T= ENSP00000358851.4:n.260-34T=
ENST00000478397.5:n.133-34T=
ENST00000479578.5:n.447-34T=
ENST00000485640.5:n.360-34T=
ENST00000495742.5:n.316-34T=
ENST00000638994.1:c.260-34T= ENSP00000491134.1:n.260-34T=
XM_011541297.1:c.260-34T= XP_011539599.1:n.260-34T=
XM_011541298.1:c.-53-34T= XP_011539600.1:n.-53-34T=
XM_017001085.1:c.260-34T= XP_016856574.1:n.260-34T=
XM_017001086.1:c.137-34T= XP_016856575.1:n.137-34T=
XM_017001087.2:c.137-34T= XP_016856576.1:n.137-34T=
XM_017001088.2:c.-53-34T= XP_016856577.1:n.-53-34T=
XM_024446577.1:c.260-34T= XP_024302345.1:n.260-34T=