Linked Data
ClinVar Variation Id:
143537
ClinVar RCV Id:
RCV000133070
dbSNP Id:
rs267608452
MyVariant Identifiers:
chrX:g.153297709dupT (hg19)
chrX:g.153297708_153297709insT (hg19)
chrX:g.154032258dupT (hg38)
chrX:g.154032257_154032258insT (hg38)
PubMed:
PMID:20031356
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154032259dup , CM000685.2:g.154032259dup | GRCh38 |
| NC_000023.10:g.153297710dup , CM000685.1:g.153297710dup | GRCh37 |
| NC_000023.9:g.152950904dup | NCBI36 |
| NG_007107.2:g.109870dup | |
| NG_007107.3:g.109846dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.326dup MANE Plus Clinical | ENSP00000301948.6:p.Gln110AlafsTer12 | |
| ENST00000453960.7:c.362dup MANE Select | ENSP00000395535.2:p.Gln122AlafsTer12 | |
| ENST00000303391.10:c.326dup | ENSP00000301948.6:p.Gln110AlafsTer12 | |
| ENST00000369957.5:c.*380dup | ENSP00000358973.4:n.*380dup | |
| ENST00000407218.5:c.362dup | ENSP00000384865.2:p.Gln122AlafsTer12 | |
| ENST00000453960.6:c.362dup | ENSP00000395535.2:p.Gln122AlafsTer12 | |
| ENST00000486506.5:n.2674dup | ||
| ENST00000611468.1:c.314dup | ENSP00000479736.1:p.Gln106AlafsTer12 | |
| ENST00000619732.4:c.326dup | ENSP00000480973.1:p.Gln110AlafsTer12 | |
| ENST00000622433.4:c.314dup | ENSP00000484470.1:p.Gln106AlafsTer12 | |
| ENST00000628176.2:c.326dup | ENSP00000486978.1:p.Gln110AlafsTer12 | |
| NM_001110792.1:c.362dup | NP_001104262.1:p.Gln122AlafsTer12 | |
| NM_001316337.1:c.47dup | NP_001303266.1:p.Gln17AlafsTer12 | |
| NM_004992.3:c.326dup | NP_004983.1:p.Gln110AlafsTer12 | |
| XM_005274681.3:c.326dup | XP_005274738.1:p.Gln110AlafsTer12 | |
| XM_005274682.3:c.47dup | XP_005274739.1:p.Gln17AlafsTer12 | |
| XM_005274683.3:c.47dup | XP_005274740.1:p.Gln17AlafsTer12 | |
| XM_011531166.1:c.47dup | XP_011529468.1:p.Gln17AlafsTer12 | |
| XM_006724819.3:c.-235dup | XP_006724882.1:n.-235dup | |
| XM_011531166.2:c.47dup | XP_011529468.1:p.Gln17AlafsTer12 | |
| XM_024452383.1:c.47dup | XP_024308151.1:p.Gln17AlafsTer12 | |
| XM_024452384.1:c.47dup | XP_024308152.1:p.Gln17AlafsTer12 | |
| NM_001110792.2:c.362dup MANE Select | NP_001104262.1:p.Gln122AlafsTer12 | |
| NM_001316337.2:c.47dup | NP_001303266.1:p.Gln17AlafsTer12 | |
| NM_001369391.2:c.47dup | NP_001356320.1:p.Gln17AlafsTer12 | |
| NM_001369392.2:c.47dup | NP_001356321.1:p.Gln17AlafsTer12 | |
| NM_001369393.2:c.47dup | NP_001356322.1:p.Gln17AlafsTer12 | |
| NM_001369394.1:c.47dup | NP_001356323.1:p.Gln17AlafsTer12 | |
| NM_001369394.2:c.47dup | NP_001356323.1:p.Gln17AlafsTer12 | |
| NM_001386137.1:c.-235dup | NP_001373066.1:n.-235dup | |
| NM_001386138.1:c.-235dup | NP_001373067.1:n.-235dup | |
| NM_001386139.1:c.-235dup | NP_001373068.1:n.-235dup | |
| NM_004992.4:c.326dup MANE Plus Clinical | NP_004983.1:p.Gln110AlafsTer12 |