Canonical Allele Identifier: CA1980215872
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586108C= , CM000673.2:g.67586108C= GRCh38
NC_000011.9:g.67353579C= , CM000673.1:g.67353579C= GRCh37
NC_000011.8:g.67110155C= NCBI36
NG_012075.1:g.7514C= , LRG_723:g.7514C=

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-281C= ENSP00000381604.1:n.337-281C=
ENST00000398606.10:c.341C= MANE Select ENSP00000381607.3:p.Ala114=
ENST00000646888.1:c.*57C= ENSP00000494477.1:n.*57C=
ENST00000398603.5:c.337-281C= ENSP00000381604.1:n.337-281C=
ENST00000398606.7:c.341C= ENSP00000381607.3:p.Ala114=
ENST00000467591.1:n.452C=
ENST00000494593.1:n.1136C=
ENST00000495996.1:c.5C= ENSP00000484686.1:p.Ala2=
ENST00000498765.5:c.404C=
NM_000852.3:c.341C= , LRG_723t1:c.341C= NP_000843.1:p.Ala114=
NM_000852.4:c.341C= MANE Select NP_000843.1:p.Ala114=