Canonical Allele Identifier: CA381521151
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134395295

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586173C>A , CM000673.2:g.67586173C>A GRCh38
NC_000011.9:g.67353644C>A , CM000673.1:g.67353644C>A GRCh37
NC_000011.8:g.67110220C>A NCBI36
NG_012075.1:g.7579C>A , LRG_723:g.7579C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-216C>A ENSP00000381604.1:n.337-216C>A
ENST00000398606.10:c.406C>A MANE Select ENSP00000381607.3:p.Gln136Lys
ENST00000646888.1:c.*122C>A ENSP00000494477.1:n.*122C>A
ENST00000398603.5:c.337-216C>A ENSP00000381604.1:n.337-216C>A
ENST00000398606.7:c.406C>A ENSP00000381607.3:p.Gln136Lys
ENST00000467591.1:n.517C>A
ENST00000494593.1:n.1201C>A
ENST00000495996.1:c.70C>A ENSP00000484686.1:p.Gln24Lys
ENST00000498765.5:c.469C>A
NM_000852.3:c.406C>A , LRG_723t1:c.406C>A NP_000843.1:p.Gln136Lys
NM_000852.4:c.406C>A MANE Select NP_000843.1:p.Gln136Lys