Canonical Allele Identifier: CA6142790

Gene: GSTP1

Linked Data

• ClinVar Variation Id: 37340
• ClinVar RCV Id: RCV000437330 ; RCV001642249 ; RCV002259310
• dbSNP Id: rs1695
• ExAC: 11:67352689 A / G
• gnomAD v2: 11-67352689-A-G
• gnomAD v3: 11-67585218-A-G
• gnomAD v4: 11-67585218-A-G
• MyVariant Identifiers: chr11:g.67352689A>G (hg19) ; chr11:g.67585218A>G (hg38)
• CIViC: CA6142790
• PubMed: PMID:15213713 ; PMID:17409936 ; PMID:19203783 ; PMID:19922504 ; PMID:20078613 ; PMID:20530282 ; PMID:20568049 ; PMID:21362365 ; PMID:21449681 ; PMID:22992668 ; PMID:23775025

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585218A>G , CM000673.2:g.67585218A>G	GRCh38
NC_000011.9:g.67352689A>G , CM000673.1:g.67352689A>G	GRCh37
NC_000011.8:g.67109265A>G	NCBI36
NG_012075.1:g.6624A>G , LRG_723:g.6624A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.313A>G	ENSP00000381604.1:p.Ile105Val
ENST00000398606.10:c.313A>G MANE Select	ENSP00000381607.3:p.Ile105Val
ENST00000646888.1:c.*29A>G	ENSP00000494477.1:n.*29A>G
ENST00000398603.5:c.313A>G	ENSP00000381604.1:p.Ile105Val
ENST00000398606.7:c.313A>G	ENSP00000381607.3:p.Ile105Val
ENST00000467591.1:n.424A>G
ENST00000494593.1:n.1108A>G
ENST00000498765.5:c.376A>G
NM_000852.3:c.313A>G , LRG_723t1:c.313A>G	NP_000843.1:p.Ile105Val
NM_000852.4:c.313A>G MANE Select	NP_000843.1:p.Ile105Val