Canonical Allele Identifier: CA2614644998
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584801A>C , CM000673.2:g.67584801A>C GRCh38
NC_000011.9:g.67352272A>C , CM000673.1:g.67352272A>C GRCh37
NC_000011.8:g.67108848A>C NCBI36
NG_012075.1:g.6207A>C , LRG_723:g.6207A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+29A>C ENSP00000381604.1:n.232+29A>C
ENST00000398606.10:c.232+29A>C MANE Select ENSP00000381607.3:n.232+29A>C
ENST00000646888.1:c.125+29A>C ENSP00000494477.1:n.125+29A>C
ENST00000398603.5:c.232+29A>C ENSP00000381604.1:n.232+29A>C
ENST00000398606.7:c.232+29A>C ENSP00000381607.3:n.232+29A>C
ENST00000467591.1:n.7A>C
ENST00000489040.1:n.260A>C
ENST00000494593.1:n.691A>C
ENST00000498765.5:c.195+29A>C
NM_000852.3:c.232+29A>C , LRG_723t1:c.232+29A>C NP_000843.1:n.232+29A>C
NM_000852.4:c.232+29A>C MANE Select NP_000843.1:n.232+29A>C