Canonical Allele Identifier: CA475396477
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353979C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586508C>T , CM000673.2:g.67586508C>T GRCh38
NC_000011.9:g.67353979C>T , CM000673.1:g.67353979C>T GRCh37
NC_000011.8:g.67110555C>T NCBI36
NG_012075.1:g.7914C>T , LRG_723:g.7914C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.456C>T ENSP00000381604.1:p.Pro152=
ENST00000398606.10:c.564C>T MANE Select ENSP00000381607.3:p.Pro188=
ENST00000398603.5:c.456C>T ENSP00000381604.1:p.Pro152=
ENST00000398606.7:c.564C>T ENSP00000381607.3:p.Pro188=
ENST00000467591.1:n.675C>T
ENST00000494593.1:n.1536C>T
ENST00000498765.5:c.627C>T
NM_000852.3:c.564C>T , LRG_723t1:c.564C>T NP_000843.1:p.Pro188=
NM_000852.4:c.564C>T MANE Select NP_000843.1:p.Pro188=