Canonical Allele Identifier: CA599909278
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1268548534

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584776A>G , CM000673.2:g.67584776A>G GRCh38
NC_000011.9:g.67352247A>G , CM000673.1:g.67352247A>G GRCh37
NC_000011.8:g.67108823A>G NCBI36
NG_012075.1:g.6182A>G , LRG_723:g.6182A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+4A>G ENSP00000381604.1:n.232+4A>G
ENST00000398606.10:c.232+4A>G MANE Select ENSP00000381607.3:n.232+4A>G
ENST00000646888.1:c.125+4A>G ENSP00000494477.1:n.125+4A>G
ENST00000398603.5:c.232+4A>G ENSP00000381604.1:n.232+4A>G
ENST00000398606.7:c.232+4A>G ENSP00000381607.3:n.232+4A>G
ENST00000489040.1:n.235A>G
ENST00000494593.1:n.666A>G
ENST00000498765.5:c.195+4A>G
NM_000852.3:c.232+4A>G , LRG_723t1:c.232+4A>G NP_000843.1:n.232+4A>G
NM_000852.4:c.232+4A>G MANE Select NP_000843.1:n.232+4A>G