Canonical Allele Identifier: CA381516076
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1200793614

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584740A>G , CM000673.2:g.67584740A>G GRCh38
NC_000011.9:g.67352211A>G , CM000673.1:g.67352211A>G GRCh37
NC_000011.8:g.67108787A>G NCBI36
NG_012075.1:g.6146A>G , LRG_723:g.6146A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.200A>G ENSP00000381604.1:p.Asn67Ser
ENST00000398606.10:c.200A>G MANE Select ENSP00000381607.3:p.Asn67Ser
ENST00000646888.1:c.93A>G ENSP00000494477.1:p.Gln31=
ENST00000398603.5:c.200A>G ENSP00000381604.1:p.Asn67Ser
ENST00000398606.7:c.200A>G ENSP00000381607.3:p.Asn67Ser
ENST00000489040.1:n.199A>G
ENST00000494593.1:n.630A>G
ENST00000498765.5:c.163A>G
NM_000852.3:c.200A>G , LRG_723t1:c.200A>G NP_000843.1:p.Asn67Ser
NM_000852.4:c.200A>G MANE Select NP_000843.1:p.Asn67Ser