Canonical Allele Identifier: CA381516069
Gene: GSTP1 HGNC NCBI

Linked Data

COSMIC: COSM4402110 COSM4402111
MyVariant Identifiers: chr11:g.67352211A>C (hg19) chr11:g.67584740A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584740A>C , CM000673.2:g.67584740A>C GRCh38
NC_000011.9:g.67352211A>C , CM000673.1:g.67352211A>C GRCh37
NC_000011.8:g.67108787A>C NCBI36
NG_012075.1:g.6146A>C , LRG_723:g.6146A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.200A>C ENSP00000381604.1:p.Asn67Thr
ENST00000398606.10:c.200A>C MANE Select ENSP00000381607.3:p.Asn67Thr
ENST00000646888.1:c.93A>C ENSP00000494477.1:p.Gln31His
ENST00000398603.5:c.200A>C ENSP00000381604.1:p.Asn67Thr
ENST00000398606.7:c.200A>C ENSP00000381607.3:p.Asn67Thr
ENST00000489040.1:n.199A>C
ENST00000494593.1:n.630A>C
ENST00000498765.5:c.163A>C
NM_000852.3:c.200A>C , LRG_723t1:c.200A>C NP_000843.1:p.Asn67Thr
NM_000852.4:c.200A>C MANE Select NP_000843.1:p.Asn67Thr
Search 100 bp 5'
Search 100 bp 3'