Canonical Allele Identifier: CA381522635
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591100798

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586434G>C , CM000673.2:g.67586434G>C GRCh38
NC_000011.9:g.67353905G>C , CM000673.1:g.67353905G>C GRCh37
NC_000011.8:g.67110481G>C NCBI36
NG_012075.1:g.7840G>C , LRG_723:g.7840G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.382G>C ENSP00000381604.1:p.Glu128Gln
ENST00000398606.10:c.490G>C MANE Select ENSP00000381607.3:p.Glu164Gln
ENST00000646888.1:c.*206G>C ENSP00000494477.1:n.*206G>C
ENST00000398603.5:c.382G>C ENSP00000381604.1:p.Glu128Gln
ENST00000398606.7:c.490G>C ENSP00000381607.3:p.Glu164Gln
ENST00000467591.1:n.601G>C
ENST00000494593.1:n.1462G>C
ENST00000495996.1:c.216G>C ENSP00000484686.1:n.216G>C
ENST00000498765.5:c.553G>C
NM_000852.3:c.490G>C , LRG_723t1:c.490G>C NP_000843.1:p.Glu164Gln
NM_000852.4:c.490G>C MANE Select NP_000843.1:p.Glu164Gln