Canonical Allele Identifier: CA2580573357

Gene: GSTP1

Linked Data

• ClinVar Variation Id: 16493
• ClinVar RCV Id: RCV000017957

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.[67585218A>G;67586108C>T] , CM000673.2:g.[67585218A>G;67586108C>T]	GRCh38
NC_000011.9:g.[67352689A>G;67353579C>T] , CM000673.1:g.[67352689A>G;67353579C>T]	GRCh37
NC_000011.8:g.[67109265A>G;67110155C>T]	NCBI36
NG_012075.1:g.[6624A>G;7514C>T] , LRG_723:g.[6624A>G;7514C>T]

Transcript Alleles

HGVS	Amino-acid change
ENST00000398603.6:c.[313A>G;337-281C>T]	ENSP00000381604.1:p.Ile105Val
ENST00000398606.10:c.[313A>G;341C>T] MANE Select	ENSP00000381607.3:p.[Ile105Val;Ala114Val]...
ENST00000646888.1:c.[*29A>G;*57C>T]	ENSP00000494477.1:n.[*29A>G;*57C>T]
ENST00000398603.5:c.[313A>G;337-281C>T]	ENSP00000381604.1:p.Ile105Val
ENST00000398606.7:c.[313A>G;341C>T]	ENSP00000381607.3:p.[Ile105Val;Ala114Val]...
ENST00000467591.1:n.[424A>G;452C>T]
ENST00000494593.1:n.[1108A>G;1136C>T]
ENST00000498765.5:c.[376A>G;404C>T]
NM_000852.3:c.[313A>G;341C>T] , LRG_723t1:c.[313A>G;341C>T]	NP_000843.1:p.[Ile105Val;Ala114Val]
NM_000852.4:c.[313A>G;341C>T] MANE Select	NP_000843.1:p.[Ile105Val;Ala114Val]