Canonical Allele Identifier: CA1980215732
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586002C= , CM000673.2:g.67586002C= GRCh38
NC_000011.9:g.67353473C= , CM000673.1:g.67353473C= GRCh37
NC_000011.8:g.67110049C= NCBI36
NG_012075.1:g.7408C= , LRG_723:g.7408C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-387C= ENSP00000381604.1:n.337-387C=
ENST00000398606.10:c.337-102C= MANE Select ENSP00000381607.3:n.337-102C=
ENST00000646888.1:c.*53-102C= ENSP00000494477.1:n.*53-102C=
ENST00000398603.5:c.337-387C= ENSP00000381604.1:n.337-387C=
ENST00000398606.7:c.337-102C= ENSP00000381607.3:n.337-102C=
ENST00000467591.1:n.448-102C=
ENST00000494593.1:n.1132-102C=
ENST00000498765.5:c.400-102C=
NM_000852.3:c.337-102C= , LRG_723t1:c.337-102C= NP_000843.1:n.337-102C=
NM_000852.4:c.337-102C= MANE Select NP_000843.1:n.337-102C=