Canonical Allele Identifier: CA1980216192
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586300G= , CM000673.2:g.67586300G= GRCh38
NC_000011.9:g.67353771G= , CM000673.1:g.67353771G= GRCh37
NC_000011.8:g.67110347G= NCBI36
NG_012075.1:g.7706G= , LRG_723:g.7706G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-89G= ENSP00000381604.1:n.337-89G=
ENST00000398606.10:c.445-89G= MANE Select ENSP00000381607.3:n.445-89G=
ENST00000646888.1:c.*161-89G= ENSP00000494477.1:n.*161-89G=
ENST00000398603.5:c.337-89G= ENSP00000381604.1:n.337-89G=
ENST00000398606.7:c.445-89G= ENSP00000381607.3:n.445-89G=
ENST00000467591.1:n.556-89G=
ENST00000494593.1:n.1328G=
ENST00000495996.1:c.170+27G= ENSP00000484686.1:n.170+27G=
ENST00000498765.5:c.508-89G=
NM_000852.3:c.445-89G= , LRG_723t1:c.445-89G= NP_000843.1:n.445-89G=
NM_000852.4:c.445-89G= MANE Select NP_000843.1:n.445-89G=