Canonical Allele Identifier: CA475394633
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352188A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584717A>T , CM000673.2:g.67584717A>T GRCh38
NC_000011.9:g.67352188A>T , CM000673.1:g.67352188A>T GRCh37
NC_000011.8:g.67108764A>T NCBI36
NG_012075.1:g.6123A>T , LRG_723:g.6123A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.177A>T ENSP00000381604.1:p.Gly59=
ENST00000398606.10:c.177A>T MANE Select ENSP00000381607.3:p.Gly59=
ENST00000646888.1:c.70A>T ENSP00000494477.1:p.Arg24Ter
ENST00000398603.5:c.177A>T ENSP00000381604.1:p.Gly59=
ENST00000398606.7:c.177A>T ENSP00000381607.3:p.Gly59=
ENST00000489040.1:n.176A>T
ENST00000494593.1:n.607A>T
ENST00000498765.5:c.140A>T
NM_000852.3:c.177A>T , LRG_723t1:c.177A>T NP_000843.1:p.Gly59=
NM_000852.4:c.177A>T MANE Select NP_000843.1:p.Gly59=