Canonical Allele Identifier: CA939080958
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1867451954

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585447_67585448del , CM000673.2:g.67585447_67585448del GRCh38
NC_000011.9:g.67352918_67352919del , CM000673.1:g.67352918_67352919del GRCh37
NC_000011.8:g.67109494_67109495del NCBI36
NG_012075.1:g.6853_6854del , LRG_723:g.6853_6854del

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+206_336+207del ENSP00000381604.1:n.336+206_336+207del
ENST00000398606.10:c.336+206_336+207del MANE Select ENSP00000381607.3:n.336+206_336+207del
ENST00000646888.1:c.*52+206_*52+207del ENSP00000494477.1:n.*52+206_*52+207del
ENST00000398603.5:c.336+206_336+207del ENSP00000381604.1:n.336+206_336+207del
ENST00000398606.7:c.336+206_336+207del ENSP00000381607.3:n.336+206_336+207del
ENST00000467591.1:n.447+206_447+207del
ENST00000494593.1:n.1131+206_1131+207del
ENST00000498765.5:c.399+206_399+207del
NM_000852.3:c.336+206_336+207del , LRG_723t1:c.336+206_336+207del NP_000843.1:n.336+206_336+207del
NM_000852.4:c.336+206_336+207del MANE Select NP_000843.1:n.336+206_336+207del