Canonical Allele Identifier: CA1980215089
Gene: GSTP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585458A= , CM000673.2:g.67585458A= GRCh38
NC_000011.9:g.67352929A= , CM000673.1:g.67352929A= GRCh37
NC_000011.8:g.67109505A= NCBI36
NG_012075.1:g.6864A= , LRG_723:g.6864A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+217A= ENSP00000381604.1:n.336+217A=
ENST00000398606.10:c.336+217A= MANE Select ENSP00000381607.3:n.336+217A=
ENST00000646888.1:c.*52+217A= ENSP00000494477.1:n.*52+217A=
ENST00000398603.5:c.336+217A= ENSP00000381604.1:n.336+217A=
ENST00000398606.7:c.336+217A= ENSP00000381607.3:n.336+217A=
ENST00000467591.1:n.447+217A=
ENST00000494593.1:n.1131+217A=
ENST00000498765.5:c.399+217A=
NM_000852.3:c.336+217A= , LRG_723t1:c.336+217A= NP_000843.1:n.336+217A=
NM_000852.4:c.336+217A= MANE Select NP_000843.1:n.336+217A=
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