Canonical Allele Identifier: CA775384354

Gene: TIMP2

Linked Data

• dbSNP Id: rs1363874384
• gnomAD v3: 17-78870612-G-GCCTC
• gnomAD v4: 17-78870612-G-GCCTC
• MyVariant Identifiers: chr17:g.76866694_76866695insCCTC (hg19) ; chr17:g.78870612_78870613insCCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78870613_78870614insCTCC , CM000679.2:g.78870613_78870614insCTCC	GRCh38
NC_000017.10:g.76866695_76866696insCTCC , CM000679.1:g.76866695_76866696insCTCC	GRCh37
NC_000017.9:g.74378290_74378291insCTCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586713.6:c.109+285_109+286insGAGG	ENSP00000465968.2:n.109+285_109+286insGAGG
ENST00000706922.1:c.109+285_109+286insGAGG	ENSP00000516642.1:n.109+285_109+286insGAGG
ENST00000706923.1:c.109+285_109+286insGAGG	ENSP00000516643.1:n.109+285_109+286insGAGG
ENST00000262768.11:c.340+285_340+286insGAGG MANE Select	ENSP00000262768.6:n.340+285_340+286insGAGG
ENST00000536189.6:c.109+285_109+286insGAGG	ENSP00000441724.1:n.109+285_109+286insGAGG
ENST00000585421.5:c.109+285_109+286insGAGG	ENSP00000467584.1:n.109+285_109+286insGAGG
ENST00000586057.5:c.109+285_109+286insGAGG	ENSP00000468296.1:n.109+285_109+286insGAGG
ENST00000592761.2:c.109+285_109+286insGAGG	ENSP00000464930.1:n.109+285_109+286insGAGG
NM_003255.4:c.340+285_340+286insGAGG	NP_003246.1:n.340+285_340+286insGAGG
NM_003255.5:c.340+285_340+286insGAGG MANE Select	NP_003246.1:n.340+285_340+286insGAGG