Canonical Allele Identifier: CA2724398785
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134395416

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586299A>G , CM000673.2:g.67586299A>G GRCh38
NC_000011.9:g.67353770A>G , CM000673.1:g.67353770A>G GRCh37
NC_000011.8:g.67110346A>G NCBI36
NG_012075.1:g.7705A>G , LRG_723:g.7705A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-90A>G ENSP00000381604.1:n.337-90A>G
ENST00000398606.10:c.444+88A>G MANE Select ENSP00000381607.3:n.444+88A>G
ENST00000646888.1:c.*160+88A>G ENSP00000494477.1:n.*160+88A>G
ENST00000398603.5:c.337-90A>G ENSP00000381604.1:n.337-90A>G
ENST00000398606.7:c.444+88A>G ENSP00000381607.3:n.444+88A>G
ENST00000467591.1:n.555+88A>G
ENST00000494593.1:n.1327A>G
ENST00000495996.1:c.170+26A>G ENSP00000484686.1:n.170+26A>G
ENST00000498765.5:c.507+88A>G
NM_000852.3:c.444+88A>G , LRG_723t1:c.444+88A>G NP_000843.1:n.444+88A>G
NM_000852.4:c.444+88A>G MANE Select NP_000843.1:n.444+88A>G