Canonical Allele Identifier: CA6142790
Gene: GSTP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37340
dbSNP Id: rs1695

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585218A>G , CM000673.2:g.67585218A>G GRCh38
NC_000011.9:g.67352689A>G , CM000673.1:g.67352689A>G GRCh37
NC_000011.8:g.67109265A>G NCBI36
NG_012075.1:g.6624A>G , LRG_723:g.6624A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.313A>G ENSP00000381604.1:p.Ile105Val
ENST00000398606.10:c.313A>G MANE Select ENSP00000381607.3:p.Ile105Val
ENST00000646888.1:c.*29A>G ENSP00000494477.1:p.=
ENST00000398603.5:c.313A>G ENSP00000381604.1:p.Ile105Val
ENST00000398606.7:c.313A>G ENSP00000381607.3:p.Ile105Val
ENST00000467591.1:n.424A>G
ENST00000494593.1:n.1108A>G
ENST00000498765.5:n.376A>G
NM_000852.3:c.313A>G , LRG_723t1:c.313A>G NP_000843.1:p.Ile105Val
NM_000852.4:c.313A>G MANE Select NP_000843.1:p.Ile105Val