Canonical Allele Identifier: CA1980215224
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585638_67585639delinsGA , CM000673.2:g.67585638_67585639delinsGA GRCh38
NC_000011.9:g.67353109_67353110delinsGA , CM000673.1:g.67353109_67353110delinsGA GRCh37
NC_000011.8:g.67109685_67109686delinsGA NCBI36
NG_012075.1:g.7044_7045delinsGA , LRG_723:g.7044_7045delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.336+397_336+398delinsGA ENSP00000381604.1:n.336+397_336+398delinsGA
ENST00000398606.10:c.336+397_336+398delinsGA MANE Select ENSP00000381607.3:n.336+397_336+398delinsGA
ENST00000646888.1:c.*52+397_*52+398delinsGA ENSP00000494477.1:n.*52+397_*52+398delinsGA
ENST00000398603.5:c.336+397_336+398delinsGA ENSP00000381604.1:n.336+397_336+398delinsGA
ENST00000398606.7:c.336+397_336+398delinsGA ENSP00000381607.3:n.336+397_336+398delinsGA
ENST00000467591.1:n.447+397_447+398delinsGA
ENST00000494593.1:n.1131+397_1131+398delinsGA
ENST00000498765.5:c.399+397_399+398delinsGA
NM_000852.3:c.336+397_336+398delinsGA , LRG_723t1:c.336+397_336+398delinsGA NP_000843.1:n.336+397_336+398delinsGA
NM_000852.4:c.336+397_336+398delinsGA MANE Select NP_000843.1:n.336+397_336+398delinsGA