Canonical Allele Identifier: CA381520592
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353597T>A (hg19) chr11:g.67586126T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586126T>A , CM000673.2:g.67586126T>A GRCh38
NC_000011.9:g.67353597T>A , CM000673.1:g.67353597T>A GRCh37
NC_000011.8:g.67110173T>A NCBI36
NG_012075.1:g.7532T>A , LRG_723:g.7532T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-263T>A ENSP00000381604.1:n.337-263T>A
ENST00000398606.10:c.359T>A MANE Select ENSP00000381607.3:p.Val120Glu
ENST00000646888.1:c.*75T>A ENSP00000494477.1:n.*75T>A
ENST00000398603.5:c.337-263T>A ENSP00000381604.1:n.337-263T>A
ENST00000398606.7:c.359T>A ENSP00000381607.3:p.Val120Glu
ENST00000467591.1:n.470T>A
ENST00000494593.1:n.1154T>A
ENST00000495996.1:c.23T>A ENSP00000484686.1:p.Val8Glu
ENST00000498765.5:c.422T>A
NM_000852.3:c.359T>A , LRG_723t1:c.359T>A NP_000843.1:p.Val120Glu
NM_000852.4:c.359T>A MANE Select NP_000843.1:p.Val120Glu
Search 100 bp 5'
Search 100 bp 3'