Canonical Allele Identifier: CA475396416
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591100881
MyVariant Identifiers: chr11:g.67353952A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586481A>C , CM000673.2:g.67586481A>C GRCh38
NC_000011.9:g.67353952A>C , CM000673.1:g.67353952A>C GRCh37
NC_000011.8:g.67110528A>C NCBI36
NG_012075.1:g.7887A>C , LRG_723:g.7887A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.429A>C ENSP00000381604.1:p.Ala143=
ENST00000398606.10:c.537A>C MANE Select ENSP00000381607.3:p.Ala179=
ENST00000646888.1:c.*253A>C ENSP00000494477.1:n.*253A>C
ENST00000398603.5:c.429A>C ENSP00000381604.1:p.Ala143=
ENST00000398606.7:c.537A>C ENSP00000381607.3:p.Ala179=
ENST00000467591.1:n.648A>C
ENST00000494593.1:n.1509A>C
ENST00000498765.5:c.600A>C
NM_000852.3:c.537A>C , LRG_723t1:c.537A>C NP_000843.1:p.Ala179=
NM_000852.4:c.537A>C MANE Select NP_000843.1:p.Ala179=
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Search 100 bp 3'