Canonical Allele Identifier: CA475396524
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67354006T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586535T>A , CM000673.2:g.67586535T>A GRCh38
NC_000011.9:g.67354006T>A , CM000673.1:g.67354006T>A GRCh37
NC_000011.8:g.67110582T>A NCBI36
NG_012075.1:g.7941T>A , LRG_723:g.7941T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.483T>A ENSP00000381604.1:p.Pro161=
ENST00000398606.10:c.591T>A MANE Select ENSP00000381607.3:p.Pro197=
ENST00000398603.5:c.483T>A ENSP00000381604.1:p.Pro161=
ENST00000398606.7:c.591T>A ENSP00000381607.3:p.Pro197=
ENST00000467591.1:n.702T>A
ENST00000494593.1:n.1563T>A
ENST00000498765.5:c.654T>A
NM_000852.3:c.591T>A , LRG_723t1:c.591T>A NP_000843.1:p.Pro197=
NM_000852.4:c.591T>A MANE Select NP_000843.1:p.Pro197=
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