Linked Data
ClinVar Variation Id:
143655
ClinVar RCV Id:
RCV000133196
dbSNP Id:
rs61749736
PubMed:
PMID:10814719
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154031150_154031151insT , CM000685.2:g.154031150_154031151insT | GRCh38 |
| NC_000023.10:g.153296601_153296602insT , CM000685.1:g.153296601_153296602insT | GRCh37 |
| NC_000023.9:g.152949795_152949796insT | NCBI36 |
| NG_007107.2:g.110977_110978insA | |
| NG_007107.3:g.110953_110954insA |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.677_678insA MANE Plus Clinical | ENSP00000301948.6:p.Phe226LeufsTer10 | |
| ENST00000453960.7:c.713_714insA MANE Select | ENSP00000395535.2:p.Phe238LeufsTer10 | |
| ENST00000637917.1:c.66-215_66-214insA | ||
| ENST00000303391.10:c.677_678insA | ENSP00000301948.6:p.Phe226LeufsTer10 | |
| ENST00000407218.5:c.*49_*50insA | ENSP00000384865.2:n.*49_*50insA | |
| ENST00000453960.6:c.713_714insA | ENSP00000395535.2:p.Phe238LeufsTer10 | |
| ENST00000619732.4:c.677_678insA | ENSP00000480973.1:p.Phe226LeufsTer10 | |
| ENST00000622433.4:c.665_666insA | ENSP00000484470.1:p.Phe222LeufsTer10 | |
| ENST00000628176.2:c.*49_*50insA | ENSP00000486978.1:n.*49_*50insA | |
| NM_001110792.1:c.713_714insA | NP_001104262.1:p.Phe238LeufsTer10 | |
| NM_001316337.1:c.398_399insA | NP_001303266.1:p.Phe133LeufsTer10 | |
| NM_004992.3:c.677_678insA | NP_004983.1:p.Phe226LeufsTer10 | |
| XM_005274681.3:c.677_678insA | XP_005274738.1:p.Phe226LeufsTer10 | |
| XM_005274682.3:c.398_399insA | XP_005274739.1:p.Phe133LeufsTer10 | |
| XM_005274683.3:c.398_399insA | XP_005274740.1:p.Phe133LeufsTer10 | |
| XM_006724819.2:c.8_9insA | XP_006724882.1:p.Phe3LeufsTer10 | |
| XM_011531166.1:c.398_399insA | XP_011529468.1:p.Phe133LeufsTer10 | |
| XM_006724819.3:c.8_9insA | XP_006724882.1:p.Phe3LeufsTer10 | |
| XM_011531166.2:c.398_399insA | XP_011529468.1:p.Phe133LeufsTer10 | |
| XM_024452383.1:c.398_399insA | XP_024308151.1:p.Phe133LeufsTer10 | |
| XM_024452384.1:c.398_399insA | XP_024308152.1:p.Phe133LeufsTer10 | |
| NM_001110792.2:c.713_714insA MANE Select | NP_001104262.1:p.Phe238LeufsTer10 | |
| NM_001316337.2:c.398_399insA | NP_001303266.1:p.Phe133LeufsTer10 | |
| NM_001369391.2:c.398_399insA | NP_001356320.1:p.Phe133LeufsTer10 | |
| NM_001369392.2:c.398_399insA | NP_001356321.1:p.Phe133LeufsTer10 | |
| NM_001369393.2:c.398_399insA | NP_001356322.1:p.Phe133LeufsTer10 | |
| NM_001369394.1:c.398_399insA | NP_001356323.1:p.Phe133LeufsTer10 | |
| NM_001369394.2:c.398_399insA | NP_001356323.1:p.Phe133LeufsTer10 | |
| NM_001386137.1:c.8_9insA | NP_001373066.1:p.Phe3LeufsTer10 | |
| NM_001386138.1:c.8_9insA | NP_001373067.1:p.Phe3LeufsTer10 | |
| NM_001386139.1:c.8_9insA | NP_001373068.1:p.Phe3LeufsTer10 | |
| NM_004992.4:c.677_678insA MANE Plus Clinical | NP_004983.1:p.Phe226LeufsTer10 |