Canonical Allele Identifier: CA1980213692
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584589G= , CM000673.2:g.67584589G= GRCh38
NC_000011.9:g.67352060G= , CM000673.1:g.67352060G= GRCh37
NC_000011.8:g.67108636G= NCBI36
NG_012075.1:g.5995G= , LRG_723:g.5995G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.144+19G= ENSP00000381604.1:n.144+19G=
ENST00000398606.10:c.144+19G= MANE Select ENSP00000381607.3:n.144+19G=
ENST00000646888.1:c.38-96G= ENSP00000494477.1:n.38-96G=
ENST00000398603.5:c.144+19G= ENSP00000381604.1:n.144+19G=
ENST00000398606.7:c.144+19G= ENSP00000381607.3:n.144+19G=
ENST00000489040.1:n.143+19G=
ENST00000494593.1:n.479G=
ENST00000498765.5:c.107+19G=
NM_000852.3:c.144+19G= , LRG_723t1:c.144+19G= NP_000843.1:n.144+19G=
NM_000852.4:c.144+19G= MANE Select NP_000843.1:n.144+19G=