Canonical Allele Identifier: CA475396365
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353931T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586460T>C , CM000673.2:g.67586460T>C GRCh38
NC_000011.9:g.67353931T>C , CM000673.1:g.67353931T>C GRCh37
NC_000011.8:g.67110507T>C NCBI36
NG_012075.1:g.7866T>C , LRG_723:g.7866T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.408T>C ENSP00000381604.1:p.Asp136=
ENST00000398606.10:c.516T>C MANE Select ENSP00000381607.3:p.Asp172=
ENST00000646888.1:c.*232T>C ENSP00000494477.1:n.*232T>C
ENST00000398603.5:c.408T>C ENSP00000381604.1:p.Asp136=
ENST00000398606.7:c.516T>C ENSP00000381607.3:p.Asp172=
ENST00000467591.1:n.627T>C
ENST00000494593.1:n.1488T>C
ENST00000498765.5:c.579T>C
NM_000852.3:c.516T>C , LRG_723t1:c.516T>C NP_000843.1:p.Asp172=
NM_000852.4:c.516T>C MANE Select NP_000843.1:p.Asp172=
Search 100 bp 5'
Search 100 bp 3'