Canonical Allele Identifier: CA475396047
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1213565628

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586178C>T , CM000673.2:g.67586178C>T GRCh38
NC_000011.9:g.67353649C>T , CM000673.1:g.67353649C>T GRCh37
NC_000011.8:g.67110225C>T NCBI36
NG_012075.1:g.7584C>T , LRG_723:g.7584C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-211C>T ENSP00000381604.1:n.337-211C>T
ENST00000398606.10:c.411C>T MANE Select ENSP00000381607.3:p.Asn137=
ENST00000646888.1:c.*127C>T ENSP00000494477.1:n.*127C>T
ENST00000398603.5:c.337-211C>T ENSP00000381604.1:n.337-211C>T
ENST00000398606.7:c.411C>T ENSP00000381607.3:p.Asn137=
ENST00000467591.1:n.522C>T
ENST00000494593.1:n.1206C>T
ENST00000495996.1:c.75C>T ENSP00000484686.1:p.Asn25=
ENST00000498765.5:c.474C>T
NM_000852.3:c.411C>T , LRG_723t1:c.411C>T NP_000843.1:p.Asn137=
NM_000852.4:c.411C>T MANE Select NP_000843.1:p.Asn137=