Canonical Allele Identifier: CA1980215976
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586162C= , CM000673.2:g.67586162C= GRCh38
NC_000011.9:g.67353633C= , CM000673.1:g.67353633C= GRCh37
NC_000011.8:g.67110209C= NCBI36
NG_012075.1:g.7568C= , LRG_723:g.7568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-227C= ENSP00000381604.1:n.337-227C=
ENST00000398606.10:c.395C= MANE Select ENSP00000381607.3:p.Thr132=
ENST00000646888.1:c.*111C= ENSP00000494477.1:n.*111C=
ENST00000398603.5:c.337-227C= ENSP00000381604.1:n.337-227C=
ENST00000398606.7:c.395C= ENSP00000381607.3:p.Thr132=
ENST00000467591.1:n.506C=
ENST00000494593.1:n.1190C=
ENST00000495996.1:c.59C= ENSP00000484686.1:p.Thr20=
ENST00000498765.5:c.458C=
NM_000852.3:c.395C= , LRG_723t1:c.395C= NP_000843.1:p.Thr132=
NM_000852.4:c.395C= MANE Select NP_000843.1:p.Thr132=