Linked Data
ClinVar Variation Id:
54586
ClinVar RCV Id:
RCV001270972
dbSNP Id:
rs397508973
MyVariant Identifiers:
chr17:g.41245051_41245060dupATGGATACTT (hg19)
chr17:g.41245050_41245051insATGGATACTT (hg19)
chr17:g.43093034_43093043dupATGGATACTT (hg38)
chr17:g.43093033_43093034insATGGATACTT (hg38)
PubMed:
PMID:11748848
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43093035_43093044dup , CM000679.2:g.43093035_43093044dup | GRCh38 |
| NC_000017.10:g.41245052_41245061dup , CM000679.1:g.41245052_41245061dup | GRCh37 |
| NC_000017.9:g.38498578_38498587dup | NCBI36 |
| NG_005905.2:g.124941_124950dup , LRG_292:g.124941_124950dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.2552_2561dup | ||
| ENST00000461574.2:c.2488_2497dup | ENSP00000417241.2:p.Leu833Ter | |
| ENST00000470026.6:c.2488_2497dup | ENSP00000419274.2:p.Leu833Ter | |
| ENST00000473961.6:c.2362_2371dup | ENSP00000420201.2:p.Leu791Ter | |
| ENST00000476777.6:c.2485_2494dup | ENSP00000417554.2:p.Leu832Ter | |
| ENST00000477152.6:c.2410_2419dup | ENSP00000419988.2:p.Leu807Ter | |
| ENST00000478531.6:c.784+1701_784+1710dup | ENSP00000420412.2:n.784+1701_784+1710dup | |
| ENST00000489037.2:c.2410_2419dup | ENSP00000420781.2:p.Leu807Ter | |
| ENST00000493919.6:c.646+1701_646+1710dup | ENSP00000418819.2:n.646+1701_646+1710dup | |
| ENST00000494123.6:c.2488_2497dup | ENSP00000419103.2:p.Leu833Ter | |
| ENST00000497488.2:c.1600_1609dup | ENSP00000418986.2:p.Leu537Ter | |
| ENST00000618469.2:c.2488_2497dup | ENSP00000478114.2:p.Leu833Ter | |
| ENST00000634433.2:c.2365_2374dup | ENSP00000489431.2:p.Leu792Ter | |
| ENST00000644379.2:c.2488_2497dup | ENSP00000496570.2:p.Leu833Ter | |
| ENST00000644555.2:c.646+1701_646+1710dup | ENSP00000494614.2:n.646+1701_646+1710dup | |
| ENST00000652672.2:c.2347_2356dup | ENSP00000498906.2:p.Leu786Ter | |
| ENST00000484087.6:c.664+1701_664+1710dup | ENSP00000419481.2:n.664+1701_664+1710dup | |
| ENST00000700182.1:c.706+1701_706+1710dup | ENSP00000514849.1:n.706+1701_706+1710dup | |
| ENST00000357654.9:c.2488_2497dup MANE Select | ENSP00000350283.3:p.Leu833Ter | |
| ENST00000471181.7:c.2488_2497dup | ENSP00000418960.2:p.Leu833Ter | |
| ENST00000352993.7:c.671-2011_671-2002dup | ENSP00000312236.5:n.671-2011_671-2002dup | |
| ENST00000354071.7:c.2488_2497dup | ENSP00000326002.7:p.Leu833Ter | |
| ENST00000357654.7:c.2488_2497dup | ENSP00000350283.3:p.Leu833Ter | |
| ENST00000461221.5:c.*2271_*2280dup | ENSP00000418548.1:n.*2271_*2280dup | |
| ENST00000468300.5:c.787+1701_787+1710dup | ENSP00000417148.1:n.787+1701_787+1710dup | |
| ENST00000471181.6:c.2488_2497dup | ENSP00000418960.2:p.Leu833Ter | |
| ENST00000478531.5:c.784+1701_784+1710dup | ENSP00000420412.1:n.784+1701_784+1710dup | |
| ENST00000484087.5:c.409+1701_409+1710dup | ENSP00000419481.1:n.409+1701_409+1710dup | |
| ENST00000487825.5:c.412+1701_412+1710dup | ENSP00000418212.1:n.412+1701_412+1710dup | |
| ENST00000491747.6:c.787+1701_787+1710dup | ENSP00000420705.2:n.787+1701_787+1710dup | |
| ENST00000493795.5:c.2347_2356dup | ENSP00000418775.1:p.Leu786Ter | |
| ENST00000493919.5:c.646+1701_646+1710dup | ENSP00000418819.1:n.646+1701_646+1710dup | |
| ENST00000586385.5:c.5-29092_5-29083dup | ENSP00000465818.1:n.5-29092_5-29083dup | |
| ENST00000591534.5:c.-43-18522_-43-18513dup | ENSP00000467329.1:n.-43-18522_-43-18513du... | |
| ENST00000591849.5:c.-99+32228_-99+32237dup | ENSP00000465347.1:n.-99+32228_-99+32237du... | |
| ENST00000634433.1:c.2365_2374dup | ENSP00000489431.1:p.Leu792Ter | |
| NM_007294.3:c.2488_2497dup , LRG_292t1:c.2488_2497dup | NP_009225.1:p.Leu833Ter | |
| NM_007297.3:c.2347_2356dup | NP_009228.2:p.Leu786Ter | |
| NM_007298.3:c.787+1701_787+1710dup | NP_009229.2:n.787+1701_787+1710dup | |
| NM_007299.3:c.787+1701_787+1710dup | NP_009230.2:n.787+1701_787+1710dup | |
| NM_007300.3:c.2488_2497dup | NP_009231.2:p.Leu833Ter | |
| NR_027676.1:n.2624_2633dup | ||
| NM_007294.4:c.2488_2497dup MANE Select | NP_009225.1:p.Leu833Ter | |
| NM_007297.4:c.2347_2356dup | NP_009228.2:p.Leu786Ter | |
| NM_007299.4:c.787+1701_787+1710dup | NP_009230.2:n.787+1701_787+1710dup | |
| NM_007300.4:c.2488_2497dup | NP_009231.2:p.Leu833Ter | |
| NR_027676.2:n.2665_2674dup |