Canonical Allele Identifier: CA381523166
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353993T>G (hg19) chr11:g.67586522T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586522T>G , CM000673.2:g.67586522T>G GRCh38
NC_000011.9:g.67353993T>G , CM000673.1:g.67353993T>G GRCh37
NC_000011.8:g.67110569T>G NCBI36
NG_012075.1:g.7928T>G , LRG_723:g.7928T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.470T>G ENSP00000381604.1:p.Phe157Cys
ENST00000398606.10:c.578T>G MANE Select ENSP00000381607.3:p.Phe193Cys
ENST00000398603.5:c.470T>G ENSP00000381604.1:p.Phe157Cys
ENST00000398606.7:c.578T>G ENSP00000381607.3:p.Phe193Cys
ENST00000467591.1:n.689T>G
ENST00000494593.1:n.1550T>G
ENST00000498765.5:c.641T>G
NM_000852.3:c.578T>G , LRG_723t1:c.578T>G NP_000843.1:p.Phe193Cys
NM_000852.4:c.578T>G MANE Select NP_000843.1:p.Phe193Cys
Search 100 bp 5'
Search 100 bp 3'