Canonical Allele Identifier: CA381522911
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586480C>G , CM000673.2:g.67586480C>G GRCh38
NC_000011.9:g.67353951C>G , CM000673.1:g.67353951C>G GRCh37
NC_000011.8:g.67110527C>G NCBI36
NG_012075.1:g.7886C>G , LRG_723:g.7886C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.428C>G ENSP00000381604.1:p.Ala143Gly
ENST00000398606.10:c.536C>G MANE Select ENSP00000381607.3:p.Ala179Gly
ENST00000646888.1:c.*252C>G ENSP00000494477.1:n.*252C>G
ENST00000398603.5:c.428C>G ENSP00000381604.1:p.Ala143Gly
ENST00000398606.7:c.536C>G ENSP00000381607.3:p.Ala179Gly
ENST00000467591.1:n.647C>G
ENST00000494593.1:n.1508C>G
ENST00000498765.5:c.599C>G
NM_000852.3:c.536C>G , LRG_723t1:c.536C>G NP_000843.1:p.Ala179Gly
NM_000852.4:c.536C>G MANE Select NP_000843.1:p.Ala179Gly