Canonical Allele Identifier: CA475396066
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353676A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586205A>T , CM000673.2:g.67586205A>T GRCh38
NC_000011.9:g.67353676A>T , CM000673.1:g.67353676A>T GRCh37
NC_000011.8:g.67110252A>T NCBI36
NG_012075.1:g.7611A>T , LRG_723:g.7611A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-184A>T ENSP00000381604.1:n.337-184A>T
ENST00000398606.10:c.438A>T MANE Select ENSP00000381607.3:p.Gly146=
ENST00000646888.1:c.*154A>T ENSP00000494477.1:n.*154A>T
ENST00000398603.5:c.337-184A>T ENSP00000381604.1:n.337-184A>T
ENST00000398606.7:c.438A>T ENSP00000381607.3:p.Gly146=
ENST00000467591.1:n.549A>T
ENST00000494593.1:n.1233A>T
ENST00000495996.1:c.102A>T ENSP00000484686.1:p.Gly34=
ENST00000498765.5:c.501A>T
NM_000852.3:c.438A>T , LRG_723t1:c.438A>T NP_000843.1:p.Gly146=
NM_000852.4:c.438A>T MANE Select NP_000843.1:p.Gly146=