Linked Data
ClinVar Variation Id:
143694
ClinVar RCV Id:
RCV000133235
dbSNP Id:
rs267608524
MyVariant Identifiers:
chrX:g.153296500_153296513dupTCGGCCTCAGCTTT (hg19)
chrX:g.153296499_153296500insTCGGCCTCAGCTTT (hg19)
chrX:g.154031049_154031062dupTCGGCCTCAGCTTT (hg38)
chrX:g.154031048_154031049insTCGGCCTCAGCTTT (hg38)
PubMed:
PMID:11313756
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154031052_154031065dup , CM000685.2:g.154031052_154031065dup | GRCh38 |
| NC_000023.10:g.153296503_153296516dup , CM000685.1:g.153296503_153296516dup | GRCh37 |
| NC_000023.9:g.152949697_152949710dup | NCBI36 |
| NG_007107.2:g.111066_111079dup | |
| NG_007107.3:g.111042_111055dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.766_779dup MANE Plus Clinical | ENSP00000301948.6:p.Asp260GlufsTer34 | |
| ENST00000453960.7:c.802_815dup MANE Select | ENSP00000395535.2:p.Asp272GlufsTer34 | |
| ENST00000637917.1:c.66-126_66-113dup | ||
| ENST00000303391.10:c.766_779dup | ENSP00000301948.6:p.Asp260GlufsTer34 | |
| ENST00000407218.5:c.*138_*151dup | ENSP00000384865.2:n.*138_*151dup | |
| ENST00000453960.6:c.802_815dup | ENSP00000395535.2:p.Asp272GlufsTer34 | |
| ENST00000619732.4:c.766_779dup | ENSP00000480973.1:p.Asp260GlufsTer34 | |
| ENST00000622433.4:c.754_767dup | ENSP00000484470.1:p.Asp256GlufsTer34 | |
| ENST00000628176.2:c.*138_*151dup | ENSP00000486978.1:n.*138_*151dup | |
| NM_001110792.1:c.802_815dup | NP_001104262.1:p.Asp272GlufsTer34 | |
| NM_001316337.1:c.487_500dup | NP_001303266.1:p.Asp167GlufsTer34 | |
| NM_004992.3:c.766_779dup | NP_004983.1:p.Asp260GlufsTer34 | |
| XM_005274681.3:c.766_779dup | XP_005274738.1:p.Asp260GlufsTer34 | |
| XM_005274682.3:c.487_500dup | XP_005274739.1:p.Asp167GlufsTer34 | |
| XM_005274683.3:c.487_500dup | XP_005274740.1:p.Asp167GlufsTer34 | |
| XM_006724819.2:c.97_110dup | XP_006724882.1:p.Asp37GlufsTer34 | |
| XM_011531166.1:c.487_500dup | XP_011529468.1:p.Asp167GlufsTer34 | |
| XM_006724819.3:c.97_110dup | XP_006724882.1:p.Asp37GlufsTer34 | |
| XM_011531166.2:c.487_500dup | XP_011529468.1:p.Asp167GlufsTer34 | |
| XM_024452383.1:c.487_500dup | XP_024308151.1:p.Asp167GlufsTer34 | |
| XM_024452384.1:c.487_500dup | XP_024308152.1:p.Asp167GlufsTer34 | |
| NM_001110792.2:c.802_815dup MANE Select | NP_001104262.1:p.Asp272GlufsTer34 | |
| NM_001316337.2:c.487_500dup | NP_001303266.1:p.Asp167GlufsTer34 | |
| NM_001369391.2:c.487_500dup | NP_001356320.1:p.Asp167GlufsTer34 | |
| NM_001369392.2:c.487_500dup | NP_001356321.1:p.Asp167GlufsTer34 | |
| NM_001369393.2:c.487_500dup | NP_001356322.1:p.Asp167GlufsTer34 | |
| NM_001369394.1:c.487_500dup | NP_001356323.1:p.Asp167GlufsTer34 | |
| NM_001369394.2:c.487_500dup | NP_001356323.1:p.Asp167GlufsTer34 | |
| NM_001386137.1:c.97_110dup | NP_001373066.1:p.Asp37GlufsTer34 | |
| NM_001386138.1:c.97_110dup | NP_001373067.1:p.Asp37GlufsTer34 | |
| NM_001386139.1:c.97_110dup | NP_001373068.1:p.Asp37GlufsTer34 | |
| NM_004992.4:c.766_779dup MANE Plus Clinical | NP_004983.1:p.Asp260GlufsTer34 |