Canonical Allele Identifier: CA475396057
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353664C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586193C>G , CM000673.2:g.67586193C>G GRCh38
NC_000011.9:g.67353664C>G , CM000673.1:g.67353664C>G GRCh37
NC_000011.8:g.67110240C>G NCBI36
NG_012075.1:g.7599C>G , LRG_723:g.7599C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-196C>G ENSP00000381604.1:n.337-196C>G
ENST00000398606.10:c.426C>G MANE Select ENSP00000381607.3:p.Thr142=
ENST00000646888.1:c.*142C>G ENSP00000494477.1:n.*142C>G
ENST00000398603.5:c.337-196C>G ENSP00000381604.1:n.337-196C>G
ENST00000398606.7:c.426C>G ENSP00000381607.3:p.Thr142=
ENST00000467591.1:n.537C>G
ENST00000494593.1:n.1221C>G
ENST00000495996.1:c.90C>G ENSP00000484686.1:p.Thr30=
ENST00000498765.5:c.489C>G
NM_000852.3:c.426C>G , LRG_723t1:c.426C>G NP_000843.1:p.Thr142=
NM_000852.4:c.426C>G MANE Select NP_000843.1:p.Thr142=
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