Canonical Allele Identifier: CA6142799
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs746579636

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585236A>G , CM000673.2:g.67585236A>G GRCh38
NC_000011.9:g.67352707A>G , CM000673.1:g.67352707A>G GRCh37
NC_000011.8:g.67109283A>G NCBI36
NG_012075.1:g.6642A>G , LRG_723:g.6642A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.331A>G ENSP00000381604.1:p.Asn111Asp
ENST00000398606.10:c.331A>G MANE Select ENSP00000381607.3:p.Asn111Asp
ENST00000646888.1:c.*47A>G ENSP00000494477.1:n.*47A>G
ENST00000398603.5:c.331A>G ENSP00000381604.1:p.Asn111Asp
ENST00000398606.7:c.331A>G ENSP00000381607.3:p.Asn111Asp
ENST00000467591.1:n.442A>G
ENST00000494593.1:n.1126A>G
ENST00000498765.5:c.394A>G
NM_000852.3:c.331A>G , LRG_723t1:c.331A>G NP_000843.1:p.Asn111Asp
NM_000852.4:c.331A>G MANE Select NP_000843.1:p.Asn111Asp