Canonical Allele Identifier: CA475395885
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353580G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586109G>T , CM000673.2:g.67586109G>T GRCh38
NC_000011.9:g.67353580G>T , CM000673.1:g.67353580G>T GRCh37
NC_000011.8:g.67110156G>T NCBI36
NG_012075.1:g.7515G>T , LRG_723:g.7515G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-280G>T ENSP00000381604.1:n.337-280G>T
ENST00000398606.10:c.342G>T MANE Select ENSP00000381607.3:p.Ala114=
ENST00000646888.1:c.*58G>T ENSP00000494477.1:n.*58G>T
ENST00000398603.5:c.337-280G>T ENSP00000381604.1:n.337-280G>T
ENST00000398606.7:c.342G>T ENSP00000381607.3:p.Ala114=
ENST00000467591.1:n.453G>T
ENST00000494593.1:n.1137G>T
ENST00000495996.1:c.6G>T ENSP00000484686.1:p.Ala2=
ENST00000498765.5:c.405G>T
NM_000852.3:c.342G>T , LRG_723t1:c.342G>T NP_000843.1:p.Ala114=
NM_000852.4:c.342G>T MANE Select NP_000843.1:p.Ala114=