Canonical Allele Identifier: CA1933495413
Community Standard Title: NM_004832.3(GSTO1):c.419C= (p.Ala140=)
Gene: GSTO1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_004832.3:c.419C= MANE Select NP_004823.1:p.Ala140=
ENST00000369713.10:c.419C= MANE Select ENSP00000358727.5:p.Ala140=
NM_001191002.1:c.367-3053C= NP_001177931.1:n.367-3053C=
NM_001191002.2:c.367-3053C= NP_001177931.1:n.367-3053C=
NM_001191003.1:c.335C= NP_001177932.1:p.Ala112=
NM_001191003.2:c.335C= NP_001177932.1:p.Ala112=
NM_004832.2:c.419C= NP_004823.1:p.Ala140=
ENST00000369710.8:c.367-3053C= ENSP00000358724.4:n.367-3053C=
ENST00000369713.9:c.419C= ENSP00000358727.5:p.Ala140=
ENST00000432659.1:c.283-3053C= ENSP00000405325.1:n.283-3053C=
ENST00000445155.5:c.335C= ENSP00000406708.1:p.Ala112=
ENST00000493946.1:n.721C=
ENST00000539281.5:c.335C= ENSP00000441488.1:p.Ala112=