Canonical Allele Identifier: CA679522880
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1476233557
MyVariant Identifiers: chr11:g.67353293T>A (hg19) chr11:g.67585822T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585822T>A , CM000673.2:g.67585822T>A GRCh38
NC_000011.9:g.67353293T>A , CM000673.1:g.67353293T>A GRCh37
NC_000011.8:g.67109869T>A NCBI36
NG_012075.1:g.7228T>A , LRG_723:g.7228T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-567T>A ENSP00000381604.1:n.337-567T>A
ENST00000398606.10:c.337-282T>A MANE Select ENSP00000381607.3:n.337-282T>A
ENST00000646888.1:c.*53-282T>A ENSP00000494477.1:n.*53-282T>A
ENST00000398603.5:c.337-567T>A ENSP00000381604.1:n.337-567T>A
ENST00000398606.7:c.337-282T>A ENSP00000381607.3:n.337-282T>A
ENST00000467591.1:n.448-282T>A
ENST00000494593.1:n.1132-282T>A
ENST00000498765.5:c.400-282T>A
NM_000852.3:c.337-282T>A , LRG_723t1:c.337-282T>A NP_000843.1:n.337-282T>A
NM_000852.4:c.337-282T>A MANE Select NP_000843.1:n.337-282T>A
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