Canonical Allele Identifier: CA475396402
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353946C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586475C>A , CM000673.2:g.67586475C>A GRCh38
NC_000011.9:g.67353946C>A , CM000673.1:g.67353946C>A GRCh37
NC_000011.8:g.67110522C>A NCBI36
NG_012075.1:g.7881C>A , LRG_723:g.7881C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.423C>A ENSP00000381604.1:p.Leu141=
ENST00000398606.10:c.531C>A MANE Select ENSP00000381607.3:p.Leu177=
ENST00000646888.1:c.*247C>A ENSP00000494477.1:n.*247C>A
ENST00000398603.5:c.423C>A ENSP00000381604.1:p.Leu141=
ENST00000398606.7:c.531C>A ENSP00000381607.3:p.Leu177=
ENST00000467591.1:n.642C>A
ENST00000494593.1:n.1503C>A
ENST00000498765.5:c.594C>A
NM_000852.3:c.531C>A , LRG_723t1:c.531C>A NP_000843.1:p.Leu177=
NM_000852.4:c.531C>A MANE Select NP_000843.1:p.Leu177=
Search 100 bp 5'
Search 100 bp 3'