Canonical Allele Identifier: CA475396409
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591100874
MyVariant Identifiers: chr11:g.67353949A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586478A>T , CM000673.2:g.67586478A>T GRCh38
NC_000011.9:g.67353949A>T , CM000673.1:g.67353949A>T GRCh37
NC_000011.8:g.67110525A>T NCBI36
NG_012075.1:g.7884A>T , LRG_723:g.7884A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.426A>T ENSP00000381604.1:p.Ser142=
ENST00000398606.10:c.534A>T MANE Select ENSP00000381607.3:p.Ser178=
ENST00000646888.1:c.*250A>T ENSP00000494477.1:n.*250A>T
ENST00000398603.5:c.426A>T ENSP00000381604.1:p.Ser142=
ENST00000398606.7:c.534A>T ENSP00000381607.3:p.Ser178=
ENST00000467591.1:n.645A>T
ENST00000494593.1:n.1506A>T
ENST00000498765.5:c.597A>T
NM_000852.3:c.534A>T , LRG_723t1:c.534A>T NP_000843.1:p.Ser178=
NM_000852.4:c.534A>T MANE Select NP_000843.1:p.Ser178=