Canonical Allele Identifier: CA1980215228
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1867454311

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585649_67585651del , CM000673.2:g.67585649_67585651del GRCh38
NC_000011.9:g.67353120_67353122del , CM000673.1:g.67353120_67353122del GRCh37
NC_000011.8:g.67109696_67109698del NCBI36
NG_012075.1:g.7055_7057del , LRG_723:g.7055_7057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+408_336+410del ENSP00000381604.1:n.336+408_336+410del
ENST00000398606.10:c.336+408_336+410del MANE Select ENSP00000381607.3:n.336+408_336+410del
ENST00000646888.1:c.*52+408_*52+410del ENSP00000494477.1:n.*52+408_*52+410del
ENST00000398603.5:c.336+408_336+410del ENSP00000381604.1:n.336+408_336+410del
ENST00000398606.7:c.336+408_336+410del ENSP00000381607.3:n.336+408_336+410del
ENST00000467591.1:n.447+408_447+410del
ENST00000494593.1:n.1131+408_1131+410del
ENST00000498765.5:c.399+408_399+410del
NM_000852.3:c.336+408_336+410del , LRG_723t1:c.336+408_336+410del NP_000843.1:n.336+408_336+410del
NM_000852.4:c.336+408_336+410del MANE Select NP_000843.1:n.336+408_336+410del