Canonical Allele Identifier: CA381522886
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353947T>A (hg19) chr11:g.67586476T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586476T>A , CM000673.2:g.67586476T>A GRCh38
NC_000011.9:g.67353947T>A , CM000673.1:g.67353947T>A GRCh37
NC_000011.8:g.67110523T>A NCBI36
NG_012075.1:g.7882T>A , LRG_723:g.7882T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.424T>A ENSP00000381604.1:p.Ser142Thr
ENST00000398606.10:c.532T>A MANE Select ENSP00000381607.3:p.Ser178Thr
ENST00000646888.1:c.*248T>A ENSP00000494477.1:n.*248T>A
ENST00000398603.5:c.424T>A ENSP00000381604.1:p.Ser142Thr
ENST00000398606.7:c.532T>A ENSP00000381607.3:p.Ser178Thr
ENST00000467591.1:n.643T>A
ENST00000494593.1:n.1504T>A
ENST00000498765.5:c.595T>A
NM_000852.3:c.532T>A , LRG_723t1:c.532T>A NP_000843.1:p.Ser178Thr
NM_000852.4:c.532T>A MANE Select NP_000843.1:p.Ser178Thr
Search 100 bp 5'
Search 100 bp 3'