Canonical Allele Identifier: CA381519099
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134394277

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585187T>G , CM000673.2:g.67585187T>G GRCh38
NC_000011.9:g.67352658T>G , CM000673.1:g.67352658T>G GRCh37
NC_000011.8:g.67109234T>G NCBI36
NG_012075.1:g.6593T>G , LRG_723:g.6593T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.282T>G ENSP00000381604.1:p.Asn94Lys
ENST00000398606.10:c.282T>G MANE Select ENSP00000381607.3:p.Asn94Lys
ENST00000646888.1:c.175T>G ENSP00000494477.1:p.Ter59Gly
ENST00000398603.5:c.282T>G ENSP00000381604.1:p.Asn94Lys
ENST00000398606.7:c.282T>G ENSP00000381607.3:p.Asn94Lys
ENST00000467591.1:n.393T>G
ENST00000494593.1:n.1077T>G
ENST00000498765.5:c.345T>G
NM_000852.3:c.282T>G , LRG_723t1:c.282T>G NP_000843.1:p.Asn94Lys
NM_000852.4:c.282T>G MANE Select NP_000843.1:p.Asn94Lys