Canonical Allele Identifier: CA1980216142
Gene: GSTP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586246C= , CM000673.2:g.67586246C= GRCh38
NC_000011.9:g.67353717C= , CM000673.1:g.67353717C= GRCh37
NC_000011.8:g.67110293C= NCBI36
NG_012075.1:g.7652C= , LRG_723:g.7652C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-143C= ENSP00000381604.1:n.337-143C=
ENST00000398606.10:c.444+35C= MANE Select ENSP00000381607.3:n.444+35C=
ENST00000646888.1:c.*160+35C= ENSP00000494477.1:n.*160+35C=
ENST00000398603.5:c.337-143C= ENSP00000381604.1:n.337-143C=
ENST00000398606.7:c.444+35C= ENSP00000381607.3:n.444+35C=
ENST00000467591.1:n.555+35C=
ENST00000494593.1:n.1274C=
ENST00000495996.1:c.143C= ENSP00000484686.1:p.Pro48=
ENST00000498765.5:c.507+35C=
NM_000852.3:c.444+35C= , LRG_723t1:c.444+35C= NP_000843.1:n.444+35C=
NM_000852.4:c.444+35C= MANE Select NP_000843.1:n.444+35C=
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