Canonical Allele Identifier: CA475396551
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67354027C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586556C>A , CM000673.2:g.67586556C>A GRCh38
NC_000011.9:g.67354027C>A , CM000673.1:g.67354027C>A GRCh37
NC_000011.8:g.67110603C>A NCBI36
NG_012075.1:g.7962C>A , LRG_723:g.7962C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.504C>A ENSP00000381604.1:p.Ile168=
ENST00000398606.10:c.612C>A MANE Select ENSP00000381607.3:p.Ile204=
ENST00000398603.5:c.504C>A ENSP00000381604.1:p.Ile168=
ENST00000398606.7:c.612C>A ENSP00000381607.3:p.Ile204=
ENST00000467591.1:n.723C>A
ENST00000494593.1:n.1584C>A
ENST00000498765.5:c.675C>A
NM_000852.3:c.612C>A , LRG_723t1:c.612C>A NP_000843.1:p.Ile204=
NM_000852.4:c.612C>A MANE Select NP_000843.1:p.Ile204=