Canonical Allele Identifier: CA885382994

Gene: GSTM4

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109658958C>G , CM000663.2:g.109658958C>G	GRCh38
NC_000001.10:g.110201580C>G , CM000663.1:g.110201580C>G	GRCh37
NC_000001.9:g.110003103C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369836.9:c.457-42C>G MANE Select	ENSP00000358851.4:n.457-42C>G
ENST00000638994.1:c.282+1164C>G	ENSP00000491134.1:n.282+1164C>G
ENST00000326729.9:c.457-42C>G	ENSP00000316471.5:n.457-42C>G
ENST00000336075.6:c.457-42C>G	ENSP00000336744.6:n.457-42C>G
ENST00000369833.5:c.334-42C>G	ENSP00000358848.1:n.334-42C>G
ENST00000369836.8:c.457-42C>G	ENSP00000358851.4:n.457-42C>G
ENST00000478397.5:n.330-42C>G
ENST00000485640.5:n.557-42C>G
ENST00000493171.5:n.637-42C>G
ENST00000493395.1:n.97-42C>G
ENST00000495742.5:n.513-42C>G
NM_000850.4:c.457-42C>G	NP_000841.1:n.457-42C>G
NM_147148.2:c.457-42C>G	NP_671489.1:n.457-42C>G
NR_024538.1:n.689-42C>G
XM_011541297.1:c.457-42C>G	XP_011539599.1:n.457-42C>G
XM_011541298.1:c.145-42C>G	XP_011539600.1:n.145-42C>G
XM_017001085.1:c.457-42C>G	XP_016856574.1:n.457-42C>G
XM_017001086.1:c.334-42C>G	XP_016856575.1:n.334-42C>G
XM_017001087.2:c.334-42C>G	XP_016856576.1:n.334-42C>G
XM_017001088.2:c.145-42C>G	XP_016856577.1:n.145-42C>G
XM_024446577.1:c.505C>G	XP_024302345.1:p.Arg169Gly
NM_000850.5:c.457-42C>G MANE Select	NP_000841.1:n.457-42C>G
NM_147148.3:c.457-42C>G	NP_671489.1:n.457-42C>G
NR_024538.2:n.666-42C>G