Canonical Allele Identifier: CA419377050

Gene: GSTM1 GSTM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109690516G>A , CM000663.2:g.109690516G>A	GRCh38
NC_000001.10:g.110233138G>A , CM000663.1:g.110233138G>A	GRCh37
NC_000001.9:g.110034661G>A	NCBI36
NG_009246.1:g.7721G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309851.10:c.519G>A (GSTM1) MANE Select	ENSP00000311469.5:p.Lys173=
ENST00000309851.9:c.519G>A (GSTM1)	ENSP00000311469.5:p.Lys173=
ENST00000349334.7:c.456+150G>A (GSTM1)	ENSP00000234981.4:n.456+150G>A
ENST00000369819.2:c.360+1191G>A (GSTM1)	ENSP00000358834.2:n.360+1191G>A
ENST00000369823.6:c.576G>A (GSTM1)	ENSP00000358838.2:p.Lys192=
ENST00000369831.6:c.568-17965G>A (GSTM2)	ENSP00000358846.2:n.568-17965G>A
ENST00000460717.7:c.*17+8682G>A (GSTM2)	ENSP00000435910.2:n.*17+8682G>A
ENST00000483399.6:c.*20+1191G>A (GSTM1)	ENSP00000455929.1:n.*20+1191G>A
ENST00000490021.2:n.344+1191G>A (GSTM1)
NM_000561.3:c.519G>A (GSTM1)	NP_000552.2:p.Lys173=
NM_146421.2:c.456+150G>A (GSTM1)	NP_666533.1:n.456+150G>A
XM_005270782.3:c.417G>A (GSTM1)	XP_005270839.1:p.Lys139=
XM_005270783.3:c.207G>A (GSTM1)	XP_005270840.1:p.Lys69=
XM_005270782.5:c.417G>A (GSTM1)	XP_005270839.1:p.Lys139=
NM_000561.4:c.519G>A (GSTM1) MANE Select	NP_000552.2:p.Lys173=
NM_146421.3:c.456+150G>A (GSTM1)	NP_666533.1:n.456+150G>A