Canonical Allele Identifier: CA2614645317
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584885C>A , CM000673.2:g.67584885C>A GRCh38
NC_000011.9:g.67352356C>A , CM000673.1:g.67352356C>A GRCh37
NC_000011.8:g.67108932C>A NCBI36
NG_012075.1:g.6291C>A , LRG_723:g.6291C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+113C>A ENSP00000381604.1:n.232+113C>A
ENST00000398606.10:c.232+113C>A MANE Select ENSP00000381607.3:n.232+113C>A
ENST00000646888.1:c.125+113C>A ENSP00000494477.1:n.125+113C>A
ENST00000398603.5:c.232+113C>A ENSP00000381604.1:n.232+113C>A
ENST00000398606.7:c.232+113C>A ENSP00000381607.3:n.232+113C>A
ENST00000467591.1:n.91C>A
ENST00000489040.1:n.344C>A
ENST00000494593.1:n.775C>A
ENST00000498765.5:c.195+113C>A
NM_000852.3:c.232+113C>A , LRG_723t1:c.232+113C>A NP_000843.1:n.232+113C>A
NM_000852.4:c.232+113C>A MANE Select NP_000843.1:n.232+113C>A