Canonical Allele Identifier: CA475396026
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353619G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586148G>A , CM000673.2:g.67586148G>A GRCh38
NC_000011.9:g.67353619G>A , CM000673.1:g.67353619G>A GRCh37
NC_000011.8:g.67110195G>A NCBI36
NG_012075.1:g.7554G>A , LRG_723:g.7554G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-241G>A ENSP00000381604.1:n.337-241G>A
ENST00000398606.10:c.381G>A MANE Select ENSP00000381607.3:p.Leu127=
ENST00000646888.1:c.*97G>A ENSP00000494477.1:n.*97G>A
ENST00000398603.5:c.337-241G>A ENSP00000381604.1:n.337-241G>A
ENST00000398606.7:c.381G>A ENSP00000381607.3:p.Leu127=
ENST00000467591.1:n.492G>A
ENST00000494593.1:n.1176G>A
ENST00000495996.1:c.45G>A ENSP00000484686.1:p.Leu15=
ENST00000498765.5:c.444G>A
NM_000852.3:c.381G>A , LRG_723t1:c.381G>A NP_000843.1:p.Leu127=
NM_000852.4:c.381G>A MANE Select NP_000843.1:p.Leu127=