Canonical Allele Identifier: CA381522690
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353917C>A (hg19) chr11:g.67586446C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586446C>A , CM000673.2:g.67586446C>A GRCh38
NC_000011.9:g.67353917C>A , CM000673.1:g.67353917C>A GRCh37
NC_000011.8:g.67110493C>A NCBI36
NG_012075.1:g.7852C>A , LRG_723:g.7852C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.394C>A ENSP00000381604.1:p.Pro132Thr
ENST00000398606.10:c.502C>A MANE Select ENSP00000381607.3:p.Pro168Thr
ENST00000646888.1:c.*218C>A ENSP00000494477.1:n.*218C>A
ENST00000398603.5:c.394C>A ENSP00000381604.1:p.Pro132Thr
ENST00000398606.7:c.502C>A ENSP00000381607.3:p.Pro168Thr
ENST00000467591.1:n.613C>A
ENST00000494593.1:n.1474C>A
ENST00000498765.5:c.565C>A
NM_000852.3:c.502C>A , LRG_723t1:c.502C>A NP_000843.1:p.Pro168Thr
NM_000852.4:c.502C>A MANE Select NP_000843.1:p.Pro168Thr
Search 100 bp 5'
Search 100 bp 3'