Canonical Allele Identifier: CA381522930
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586485G>A , CM000673.2:g.67586485G>A GRCh38
NC_000011.9:g.67353956G>A , CM000673.1:g.67353956G>A GRCh37
NC_000011.8:g.67110532G>A NCBI36
NG_012075.1:g.7891G>A , LRG_723:g.7891G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.433G>A ENSP00000381604.1:p.Val145Met
ENST00000398606.10:c.541G>A MANE Select ENSP00000381607.3:p.Val181Met
ENST00000646888.1:c.*257G>A ENSP00000494477.1:n.*257G>A
ENST00000398603.5:c.433G>A ENSP00000381604.1:p.Val145Met
ENST00000398606.7:c.541G>A ENSP00000381607.3:p.Val181Met
ENST00000467591.1:n.652G>A
ENST00000494593.1:n.1513G>A
ENST00000498765.5:c.604G>A
NM_000852.3:c.541G>A , LRG_723t1:c.541G>A NP_000843.1:p.Val181Met
NM_000852.4:c.541G>A MANE Select NP_000843.1:p.Val181Met