Canonical Allele Identifier: CA1980214299
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584937G= , CM000673.2:g.67584937G= GRCh38
NC_000011.9:g.67352408G= , CM000673.1:g.67352408G= GRCh37
NC_000011.8:g.67108984G= NCBI36
NG_012075.1:g.6343G= , LRG_723:g.6343G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+165G= ENSP00000381604.1:n.232+165G=
ENST00000398606.10:c.232+165G= MANE Select ENSP00000381607.3:n.232+165G=
ENST00000646888.1:c.125+165G= ENSP00000494477.1:n.125+165G=
ENST00000398603.5:c.232+165G= ENSP00000381604.1:n.232+165G=
ENST00000398606.7:c.232+165G= ENSP00000381607.3:n.232+165G=
ENST00000467591.1:n.143G=
ENST00000489040.1:n.396G=
ENST00000494593.1:n.827G=
ENST00000498765.5:c.196-101G=
NM_000852.3:c.232+165G= , LRG_723t1:c.232+165G= NP_000843.1:n.232+165G=
NM_000852.4:c.232+165G= MANE Select NP_000843.1:n.232+165G=