Canonical Allele Identifier: CA381518399
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352615A>C (hg19) chr11:g.67585144A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585144A>C , CM000673.2:g.67585144A>C GRCh38
NC_000011.9:g.67352615A>C , CM000673.1:g.67352615A>C GRCh37
NC_000011.8:g.67109191A>C NCBI36
NG_012075.1:g.6550A>C , LRG_723:g.6550A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.239A>C ENSP00000381604.1:p.Tyr80Ser
ENST00000398606.10:c.239A>C MANE Select ENSP00000381607.3:p.Tyr80Ser
ENST00000646888.1:c.132A>C ENSP00000494477.1:p.Leu44=
ENST00000398603.5:c.239A>C ENSP00000381604.1:p.Tyr80Ser
ENST00000398606.7:c.239A>C ENSP00000381607.3:p.Tyr80Ser
ENST00000467591.1:n.350A>C
ENST00000494593.1:n.1034A>C
ENST00000498765.5:c.302A>C
NM_000852.3:c.239A>C , LRG_723t1:c.239A>C NP_000843.1:p.Tyr80Ser
NM_000852.4:c.239A>C MANE Select NP_000843.1:p.Tyr80Ser
Search 100 bp 5'
Search 100 bp 3'