Canonical Allele Identifier: CA6142831
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs765500099

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586146C>T , CM000673.2:g.67586146C>T GRCh38
NC_000011.9:g.67353617C>T , CM000673.1:g.67353617C>T GRCh37
NC_000011.8:g.67110193C>T NCBI36
NG_012075.1:g.7552C>T , LRG_723:g.7552C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-243C>T ENSP00000381604.1:n.337-243C>T
ENST00000398606.10:c.379C>T MANE Select ENSP00000381607.3:p.Leu127=
ENST00000646888.1:c.*95C>T ENSP00000494477.1:n.*95C>T
ENST00000398603.5:c.337-243C>T ENSP00000381604.1:n.337-243C>T
ENST00000398606.7:c.379C>T ENSP00000381607.3:p.Leu127=
ENST00000467591.1:n.490C>T
ENST00000494593.1:n.1174C>T
ENST00000495996.1:c.43C>T ENSP00000484686.1:p.Leu15=
ENST00000498765.5:c.442C>T
NM_000852.3:c.379C>T , LRG_723t1:c.379C>T NP_000843.1:p.Leu127=
NM_000852.4:c.379C>T MANE Select NP_000843.1:p.Leu127=