Canonical Allele Identifier: CA381522900
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586479G>A , CM000673.2:g.67586479G>A GRCh38
NC_000011.9:g.67353950G>A , CM000673.1:g.67353950G>A GRCh37
NC_000011.8:g.67110526G>A NCBI36
NG_012075.1:g.7885G>A , LRG_723:g.7885G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.427G>A ENSP00000381604.1:p.Ala143Thr
ENST00000398606.10:c.535G>A MANE Select ENSP00000381607.3:p.Ala179Thr
ENST00000646888.1:c.*251G>A ENSP00000494477.1:n.*251G>A
ENST00000398603.5:c.427G>A ENSP00000381604.1:p.Ala143Thr
ENST00000398606.7:c.535G>A ENSP00000381607.3:p.Ala179Thr
ENST00000467591.1:n.646G>A
ENST00000494593.1:n.1507G>A
ENST00000498765.5:c.598G>A
NM_000852.3:c.535G>A , LRG_723t1:c.535G>A NP_000843.1:p.Ala179Thr
NM_000852.4:c.535G>A MANE Select NP_000843.1:p.Ala179Thr