Canonical Allele Identifier: CA2614647606
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586497_67586498del , CM000673.2:g.67586497_67586498del GRCh38
NC_000011.9:g.67353968_67353969del , CM000673.1:g.67353968_67353969del GRCh37
NC_000011.8:g.67110544_67110545del NCBI36
NG_012075.1:g.7903_7904del , LRG_723:g.7903_7904del

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.445_446del ENSP00000381604.1:p.Ser149CysfsTer13
ENST00000398606.10:c.553_554del MANE Select ENSP00000381607.3:p.Ser185CysfsTer13
ENST00000646888.1:c.*269_*270del ENSP00000494477.1:n.*269_*270del
ENST00000398603.5:c.445_446del ENSP00000381604.1:p.Ser149CysfsTer13
ENST00000398606.7:c.553_554del ENSP00000381607.3:p.Ser185CysfsTer13
ENST00000467591.1:n.664_665del
ENST00000494593.1:n.1525_1526del
ENST00000498765.5:c.616_617del
NM_000852.3:c.553_554del , LRG_723t1:c.553_554del NP_000843.1:p.Ser185CysfsTer13
NM_000852.4:c.553_554del MANE Select NP_000843.1:p.Ser185CysfsTer13