Canonical Allele Identifier: CA5681578

Gene: GSTO1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104263031C>A , CM000672.2:g.104263031C>A	GRCh38
NC_000010.10:g.106022789C>A , CM000672.1:g.106022789C>A	GRCh37
NC_000010.9:g.106012779C>A	NCBI36
NG_023362.1:g.13838C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369713.10:c.419C>A MANE Select	ENSP00000358727.5:p.Ala140Asp
ENST00000369710.8:c.367-3053C>A	ENSP00000358724.4:n.367-3053C>A
ENST00000369713.9:c.419C>A	ENSP00000358727.5:p.Ala140Asp
ENST00000432659.1:c.283-3053C>A	ENSP00000405325.1:n.283-3053C>A
ENST00000445155.5:c.335C>A	ENSP00000406708.1:p.Ala112Asp
ENST00000493946.1:n.721C>A
ENST00000539281.5:c.335C>A	ENSP00000441488.1:p.Ala112Asp
NM_001191002.1:c.367-3053C>A	NP_001177931.1:n.367-3053C>A
NM_001191003.1:c.335C>A	NP_001177932.1:p.Ala112Asp
NM_004832.2:c.419C>A	NP_004823.1:p.Ala140Asp
NM_004832.3:c.419C>A MANE Select	NP_004823.1:p.Ala140Asp
NM_001191002.2:c.367-3053C>A	NP_001177931.1:n.367-3053C>A
NM_001191003.2:c.335C>A	NP_001177932.1:p.Ala112Asp