Canonical Allele Identifier: CA6142779
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs772792333

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585121C>A , CM000673.2:g.67585121C>A GRCh38
NC_000011.9:g.67352592C>A , CM000673.1:g.67352592C>A GRCh37
NC_000011.8:g.67109168C>A NCBI36
NG_012075.1:g.6527C>A , LRG_723:g.6527C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.233-17C>A ENSP00000381604.1:n.233-17C>A
ENST00000398606.10:c.233-17C>A MANE Select ENSP00000381607.3:n.233-17C>A
ENST00000646888.1:c.126-17C>A ENSP00000494477.1:n.126-17C>A
ENST00000398603.5:c.233-17C>A ENSP00000381604.1:n.233-17C>A
ENST00000398606.7:c.233-17C>A ENSP00000381607.3:n.233-17C>A
ENST00000467591.1:n.327C>A
ENST00000494593.1:n.1011C>A
ENST00000498765.5:c.279C>A
NM_000852.3:c.233-17C>A , LRG_723t1:c.233-17C>A NP_000843.1:n.233-17C>A
NM_000852.4:c.233-17C>A MANE Select NP_000843.1:n.233-17C>A