Canonical Allele Identifier: CA2614647299
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586183del , CM000673.2:g.67586183del GRCh38
NC_000011.9:g.67353654del , CM000673.1:g.67353654del GRCh37
NC_000011.8:g.67110230del NCBI36
NG_012075.1:g.7589del , LRG_723:g.7589del

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-206del ENSP00000381604.1:n.337-206del
ENST00000398606.10:c.416del MANE Select ENSP00000381607.3:p.Gly139GlufsTer23
ENST00000646888.1:c.*132del ENSP00000494477.1:n.*132del
ENST00000398603.5:c.337-206del ENSP00000381604.1:n.337-206del
ENST00000398606.7:c.416del ENSP00000381607.3:p.Gly139GlufsTer23
ENST00000467591.1:n.527del
ENST00000494593.1:n.1211del
ENST00000495996.1:c.80del ENSP00000484686.1:p.Gly27GlufsTer11
ENST00000498765.5:c.479del
NM_000852.3:c.416del , LRG_723t1:c.416del NP_000843.1:p.Gly139GlufsTer23
NM_000852.4:c.416del MANE Select NP_000843.1:p.Gly139GlufsTer23