Linked Data
ClinVar Variation Id:
266164
ClinVar RCV Id:
RCV000257722
dbSNP Id:
rs80357770
MyVariant Identifiers:
chr17:g.41246158dupT (hg19)
chr17:g.41246157_41246158insT (hg19)
chr17:g.43094141dupT (hg38)
chr17:g.43094140_43094141insT (hg38)
PubMed:
PMID:22762150
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094144dup , CM000679.2:g.43094144dup | GRCh38 |
| NC_000017.10:g.41246161dup , CM000679.1:g.41246161dup | GRCh37 |
| NC_000017.9:g.38499687dup | NCBI36 |
| NG_005905.2:g.123843dup , LRG_292:g.123843dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.1454dup | ||
| ENST00000461574.2:c.1390dup | ENSP00000417241.2:p.Thr464AsnfsTer16 | |
| ENST00000470026.6:c.1390dup | ENSP00000419274.2:p.Thr464AsnfsTer16 | |
| ENST00000473961.6:c.1264dup | ENSP00000420201.2:p.Thr422AsnfsTer16 | |
| ENST00000476777.6:c.1387dup | ENSP00000417554.2:p.Thr463AsnfsTer16 | |
| ENST00000477152.6:c.1312dup | ENSP00000419988.2:p.Thr438AsnfsTer16 | |
| ENST00000478531.6:c.784+603dup | ENSP00000420412.2:n.784+603dup | |
| ENST00000489037.2:c.1312dup | ENSP00000420781.2:p.Thr438AsnfsTer16 | |
| ENST00000493919.6:c.646+603dup | ENSP00000418819.2:n.646+603dup | |
| ENST00000494123.6:c.1390dup | ENSP00000419103.2:p.Thr464AsnfsTer16 | |
| ENST00000497488.2:c.502dup | ENSP00000418986.2:p.Thr168AsnfsTer16 | |
| ENST00000618469.2:c.1390dup | ENSP00000478114.2:p.Thr464AsnfsTer16 | |
| ENST00000634433.2:c.1267dup | ENSP00000489431.2:p.Thr423AsnfsTer16 | |
| ENST00000644379.2:c.1390dup | ENSP00000496570.2:p.Thr464AsnfsTer16 | |
| ENST00000644555.2:c.646+603dup | ENSP00000494614.2:n.646+603dup | |
| ENST00000652672.2:c.1249dup | ENSP00000498906.2:p.Thr417AsnfsTer16 | |
| ENST00000484087.6:c.664+603dup | ENSP00000419481.2:n.664+603dup | |
| ENST00000700182.1:c.706+603dup | ENSP00000514849.1:n.706+603dup | |
| ENST00000700183.1:c.*1398dup | ENSP00000514850.1:n.*1398dup | |
| ENST00000357654.9:c.1390dup MANE Select | ENSP00000350283.3:p.Thr464AsnfsTer16 | |
| ENST00000471181.7:c.1390dup | ENSP00000418960.2:p.Thr464AsnfsTer16 | |
| ENST00000652672.1:c.1249dup | ENSP00000498906.1:p.Thr417AsnfsTer16 | |
| ENST00000352993.7:c.670+1705dup | ENSP00000312236.5:n.670+1705dup | |
| ENST00000354071.7:c.1390dup | ENSP00000326002.7:p.Thr464AsnfsTer16 | |
| ENST00000357654.7:c.1390dup | ENSP00000350283.3:p.Thr464AsnfsTer16 | |
| ENST00000412061.3:c.741dup | ||
| ENST00000461221.5:c.*1173dup | ENSP00000418548.1:n.*1173dup | |
| ENST00000468300.5:c.787+603dup | ENSP00000417148.1:n.787+603dup | |
| ENST00000470026.5:c.1390dup | ENSP00000419274.1:p.Thr464AsnfsTer16 | |
| ENST00000471181.6:c.1390dup | ENSP00000418960.2:p.Thr464AsnfsTer16 | |
| ENST00000477152.5:c.1312dup | ENSP00000419988.1:p.Thr438AsnfsTer16 | |
| ENST00000478531.5:c.784+603dup | ENSP00000420412.1:n.784+603dup | |
| ENST00000484087.5:c.409+603dup | ENSP00000419481.1:n.409+603dup | |
| ENST00000487825.5:c.412+603dup | ENSP00000418212.1:n.412+603dup | |
| ENST00000491747.6:c.787+603dup | ENSP00000420705.2:n.787+603dup | |
| ENST00000492859.5:c.*1326dup | ENSP00000420253.1:n.*1326dup | |
| ENST00000493795.5:c.1249dup | ENSP00000418775.1:p.Thr417AsnfsTer16 | |
| ENST00000493919.5:c.646+603dup | ENSP00000418819.1:n.646+603dup | |
| ENST00000494123.5:c.1390dup | ENSP00000419103.1:p.Thr464AsnfsTer? | |
| ENST00000497488.1:c.502dup | ENSP00000418986.1:p.Thr168AsnfsTer? | |
| ENST00000586385.5:c.5-30190dup | ENSP00000465818.1:n.5-30190dup | |
| ENST00000591534.5:c.-43-19620dup | ENSP00000467329.1:n.-43-19620dup | |
| ENST00000591849.5:c.-99+31130dup | ENSP00000465347.1:n.-99+31130dup | |
| ENST00000634433.1:c.1267dup | ENSP00000489431.1:p.Thr423AsnfsTer16 | |
| NM_007294.3:c.1390dup , LRG_292t1:c.1390dup | NP_009225.1:p.Thr464AsnfsTer16 | |
| NM_007297.3:c.1249dup | NP_009228.2:p.Thr417AsnfsTer16 | |
| NM_007298.3:c.787+603dup | NP_009229.2:n.787+603dup | |
| NM_007299.3:c.787+603dup | NP_009230.2:n.787+603dup | |
| NM_007300.3:c.1390dup | NP_009231.2:p.Thr464AsnfsTer16 | |
| NR_027676.1:n.1526dup | ||
| NM_007294.4:c.1390dup MANE Select | NP_009225.1:p.Thr464AsnfsTer16 | |
| NM_007297.4:c.1249dup | NP_009228.2:p.Thr417AsnfsTer16 | |
| NM_007299.4:c.787+603dup | NP_009230.2:n.787+603dup | |
| NM_007300.4:c.1390dup | NP_009231.2:p.Thr464AsnfsTer16 | |
| NR_027676.2:n.1567dup |