Canonical Allele Identifier: CA381518837
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352642T>A (hg19) chr11:g.67585171T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585171T>A , CM000673.2:g.67585171T>A GRCh38
NC_000011.9:g.67352642T>A , CM000673.1:g.67352642T>A GRCh37
NC_000011.8:g.67109218T>A NCBI36
NG_012075.1:g.6577T>A , LRG_723:g.6577T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.266T>A ENSP00000381604.1:p.Leu89Gln
ENST00000398606.10:c.266T>A MANE Select ENSP00000381607.3:p.Leu89Gln
ENST00000646888.1:c.159T>A ENSP00000494477.1:p.Pro53=
ENST00000398603.5:c.266T>A ENSP00000381604.1:p.Leu89Gln
ENST00000398606.7:c.266T>A ENSP00000381607.3:p.Leu89Gln
ENST00000467591.1:n.377T>A
ENST00000494593.1:n.1061T>A
ENST00000498765.5:c.329T>A
NM_000852.3:c.266T>A , LRG_723t1:c.266T>A NP_000843.1:p.Leu89Gln
NM_000852.4:c.266T>A MANE Select NP_000843.1:p.Leu89Gln
Search 100 bp 5'
Search 100 bp 3'