Linked Data
ClinVar Variation Id:
54939
dbSNP Id:
rs397509087
MyVariant Identifiers:
chr17:g.41243922_41243927delinsTT (hg19)
chr17:g.43091905_43091910delinsTT (hg38)
PubMed:
PMID:18489799
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43091905_43091910delinsTT , CM000679.2:g.43091905_43091910delinsTT | GRCh38 |
| NC_000017.10:g.41243922_41243927delinsTT , CM000679.1:g.41243922_41243927delinsTT | GRCh37 |
| NC_000017.9:g.38497448_38497453delinsTT | NCBI36 |
| NG_005905.2:g.126074_126079delinsAA , LRG_292:g.126074_126079delinsAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3685_3690delinsAA | ||
| ENST00000461574.2:c.3621_3626delinsAA | ENSP00000417241.2:p.Leu1209SerfsTer25 | |
| ENST00000470026.6:c.3621_3626delinsAA | ENSP00000419274.2:p.Leu1209SerfsTer25 | |
| ENST00000473961.6:c.3495_3500delinsAA | ENSP00000420201.2:p.Leu1167SerfsTer25 | |
| ENST00000476777.6:c.3618_3623delinsAA | ENSP00000417554.2:p.Leu1208SerfsTer25 | |
| ENST00000477152.6:c.3543_3548delinsAA | ENSP00000419988.2:p.Leu1183SerfsTer25 | |
| ENST00000478531.6:c.785-878_785-873delinsAA | ENSP00000420412.2:n.785-878_785-873delinsAA | |
| ENST00000489037.2:c.3543_3548delinsAA | ENSP00000420781.2:p.Leu1183SerfsTer25 | |
| ENST00000493919.6:c.647-878_647-873delinsAA | ENSP00000418819.2:n.647-878_647-873delinsAA | |
| ENST00000494123.6:c.3621_3626delinsAA | ENSP00000419103.2:p.Leu1209SerfsTer25 | |
| ENST00000497488.2:c.2733_2738delinsAA | ENSP00000418986.2:p.Leu913SerfsTer25 | |
| ENST00000618469.2:c.3621_3626delinsAA | ENSP00000478114.2:p.Leu1209SerfsTer25 | |
| ENST00000634433.2:c.3498_3503delinsAA | ENSP00000489431.2:p.Leu1168SerfsTer25 | |
| ENST00000644379.2:c.3621_3626delinsAA | ENSP00000496570.2:p.Leu1209SerfsTer25 | |
| ENST00000644555.2:c.647-878_647-873delinsAA | ENSP00000494614.2:n.647-878_647-873delinsAA | |
| ENST00000652672.2:c.3480_3485delinsAA | ENSP00000498906.2:p.Leu1162SerfsTer25 | |
| ENST00000484087.6:c.665-878_665-873delinsAA | ENSP00000419481.2:n.665-878_665-873delinsAA | |
| ENST00000700182.1:c.707-878_707-873delinsAA | ENSP00000514849.1:n.707-878_707-873delinsAA | |
| ENST00000357654.9:c.3621_3626delinsAA MANE Select | ENSP00000350283.3:p.Leu1209SerfsTer25 | |
| ENST00000471181.7:c.3621_3626delinsAA | ENSP00000418960.2:p.Leu1209SerfsTer25 | |
| ENST00000352993.7:c.671-878_671-873delinsAA | ENSP00000312236.5:n.671-878_671-873delinsAA | |
| ENST00000354071.7:c.3621_3626delinsAA | ENSP00000326002.7:p.Leu1209SerfsTer25 | |
| ENST00000357654.7:c.3621_3626delinsAA | ENSP00000350283.3:p.Leu1209SerfsTer25 | |
| ENST00000461221.5:c.*3404_*3409delinsAA | ENSP00000418548.1:n.*3404_*3409delinsAA | |
| ENST00000468300.5:c.788-878_788-873delinsAA | ENSP00000417148.1:n.788-878_788-873delinsAA | |
| ENST00000471181.6:c.3621_3626delinsAA | ENSP00000418960.2:p.Leu1209SerfsTer25 | |
| ENST00000478531.5:c.785-878_785-873delinsAA | ENSP00000420412.1:n.785-878_785-873delinsAA | |
| ENST00000484087.5:c.410-878_410-873delinsAA | ENSP00000419481.1:n.410-878_410-873delinsAA | |
| ENST00000487825.5:c.413-878_413-873delinsAA | ENSP00000418212.1:n.413-878_413-873delinsAA | |
| ENST00000491747.6:c.788-878_788-873delinsAA | ENSP00000420705.2:n.788-878_788-873delinsAA | |
| ENST00000493795.5:c.3480_3485delinsAA | ENSP00000418775.1:p.Leu1162SerfsTer25 | |
| ENST00000493919.5:c.647-878_647-873delinsAA | ENSP00000418819.1:n.647-878_647-873delinsAA | |
| ENST00000586385.5:c.5-27959_5-27954delinsAA | ENSP00000465818.1:n.5-27959_5-27954delinsAA | |
| ENST00000591534.5:c.-43-17389_-43-17384delinsAA | ENSP00000467329.1:n.-43-17389_-43-17384delinsAA | |
| ENST00000591849.5:c.-99+33361_-99+33366delinsAA | ENSP00000465347.1:n.-99+33361_-99+33366delinsAA | |
| NM_007294.3:c.3621_3626delinsAA , LRG_292t1:c.3621_3626delinsAA | NP_009225.1:p.Leu1209SerfsTer25 | |
| NM_007297.3:c.3480_3485delinsAA | NP_009228.2:p.Leu1162SerfsTer25 | |
| NM_007298.3:c.788-878_788-873delinsAA | NP_009229.2:n.788-878_788-873delinsAA | |
| NM_007299.3:c.788-878_788-873delinsAA | NP_009230.2:n.788-878_788-873delinsAA | |
| NM_007300.3:c.3621_3626delinsAA | NP_009231.2:p.Leu1209SerfsTer25 | |
| NR_027676.1:n.3757_3762delinsAA | ||
| NM_007294.4:c.3621_3626delinsAA MANE Select | NP_009225.1:p.Leu1209SerfsTer25 | |
| NM_007297.4:c.3480_3485delinsAA | NP_009228.2:p.Leu1162SerfsTer25 | |
| NM_007299.4:c.788-878_788-873delinsAA | NP_009230.2:n.788-878_788-873delinsAA | |
| NM_007300.4:c.3621_3626delinsAA | NP_009231.2:p.Leu1209SerfsTer25 | |
| NR_027676.2:n.3798_3803delinsAA |