Canonical Allele Identifier: CA475396030
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353625T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586154T>A , CM000673.2:g.67586154T>A GRCh38
NC_000011.9:g.67353625T>A , CM000673.1:g.67353625T>A GRCh37
NC_000011.8:g.67110201T>A NCBI36
NG_012075.1:g.7560T>A , LRG_723:g.7560T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-235T>A ENSP00000381604.1:n.337-235T>A
ENST00000398606.10:c.387T>A MANE Select ENSP00000381607.3:p.Pro129=
ENST00000646888.1:c.*103T>A ENSP00000494477.1:n.*103T>A
ENST00000398603.5:c.337-235T>A ENSP00000381604.1:n.337-235T>A
ENST00000398606.7:c.387T>A ENSP00000381607.3:p.Pro129=
ENST00000467591.1:n.498T>A
ENST00000494593.1:n.1182T>A
ENST00000495996.1:c.51T>A ENSP00000484686.1:p.Pro17=
ENST00000498765.5:c.450T>A
NM_000852.3:c.387T>A , LRG_723t1:c.387T>A NP_000843.1:p.Pro129=
NM_000852.4:c.387T>A MANE Select NP_000843.1:p.Pro129=