Canonical Allele Identifier: CA475396283
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353901C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586430C>A , CM000673.2:g.67586430C>A GRCh38
NC_000011.9:g.67353901C>A , CM000673.1:g.67353901C>A GRCh37
NC_000011.8:g.67110477C>A NCBI36
NG_012075.1:g.7836C>A , LRG_723:g.7836C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.378C>A ENSP00000381604.1:p.Ile126=
ENST00000398606.10:c.486C>A MANE Select ENSP00000381607.3:p.Ile162=
ENST00000646888.1:c.*202C>A ENSP00000494477.1:n.*202C>A
ENST00000398603.5:c.378C>A ENSP00000381604.1:p.Ile126=
ENST00000398606.7:c.486C>A ENSP00000381607.3:p.Ile162=
ENST00000467591.1:n.597C>A
ENST00000494593.1:n.1458C>A
ENST00000495996.1:c.212C>A ENSP00000484686.1:n.212C>A
ENST00000498765.5:c.549C>A
NM_000852.3:c.486C>A , LRG_723t1:c.486C>A NP_000843.1:p.Ile162=
NM_000852.4:c.486C>A MANE Select NP_000843.1:p.Ile162=