Canonical Allele Identifier: CA1980216022
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586189A= , CM000673.2:g.67586189A= GRCh38
NC_000011.9:g.67353660A= , CM000673.1:g.67353660A= GRCh37
NC_000011.8:g.67110236A= NCBI36
NG_012075.1:g.7595A= , LRG_723:g.7595A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-200A= ENSP00000381604.1:n.337-200A=
ENST00000398606.10:c.422A= MANE Select ENSP00000381607.3:p.Lys141=
ENST00000646888.1:c.*138A= ENSP00000494477.1:n.*138A=
ENST00000398603.5:c.337-200A= ENSP00000381604.1:n.337-200A=
ENST00000398606.7:c.422A= ENSP00000381607.3:p.Lys141=
ENST00000467591.1:n.533A=
ENST00000494593.1:n.1217A=
ENST00000495996.1:c.86A= ENSP00000484686.1:p.Lys29=
ENST00000498765.5:c.485A=
NM_000852.3:c.422A= , LRG_723t1:c.422A= NP_000843.1:p.Lys141=
NM_000852.4:c.422A= MANE Select NP_000843.1:p.Lys141=