Canonical Allele Identifier: CA381519961
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134394447

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585238C>G , CM000673.2:g.67585238C>G GRCh38
NC_000011.9:g.67352709C>G , CM000673.1:g.67352709C>G GRCh37
NC_000011.8:g.67109285C>G NCBI36
NG_012075.1:g.6644C>G , LRG_723:g.6644C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.333C>G ENSP00000381604.1:p.Asn111Lys
ENST00000398606.10:c.333C>G MANE Select ENSP00000381607.3:p.Asn111Lys
ENST00000646888.1:c.*49C>G ENSP00000494477.1:n.*49C>G
ENST00000398603.5:c.333C>G ENSP00000381604.1:p.Asn111Lys
ENST00000398606.7:c.333C>G ENSP00000381607.3:p.Asn111Lys
ENST00000467591.1:n.444C>G
ENST00000494593.1:n.1128C>G
ENST00000498765.5:c.396C>G
NM_000852.3:c.333C>G , LRG_723t1:c.333C>G NP_000843.1:p.Asn111Lys
NM_000852.4:c.333C>G MANE Select NP_000843.1:p.Asn111Lys