Canonical Allele Identifier: CA6142810
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs766397063

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586065A>G , CM000673.2:g.67586065A>G GRCh38
NC_000011.9:g.67353536A>G , CM000673.1:g.67353536A>G GRCh37
NC_000011.8:g.67110112A>G NCBI36
NG_012075.1:g.7471A>G , LRG_723:g.7471A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-324A>G ENSP00000381604.1:n.337-324A>G
ENST00000398606.10:c.337-39A>G MANE Select ENSP00000381607.3:n.337-39A>G
ENST00000646888.1:c.*53-39A>G ENSP00000494477.1:n.*53-39A>G
ENST00000398603.5:c.337-324A>G ENSP00000381604.1:n.337-324A>G
ENST00000398606.7:c.337-39A>G ENSP00000381607.3:n.337-39A>G
ENST00000467591.1:n.448-39A>G
ENST00000494593.1:n.1132-39A>G
ENST00000498765.5:c.400-39A>G
NM_000852.3:c.337-39A>G , LRG_723t1:c.337-39A>G NP_000843.1:n.337-39A>G
NM_000852.4:c.337-39A>G MANE Select NP_000843.1:n.337-39A>G