Linked Data
ClinVar Variation Id:
1143847
ClinVar RCV Id:
RCV001482136
dbSNP Id:
rs2131679212
gnomAD v4:
9-132900347-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132900348del , CM000671.2:g.132900348del | GRCh38 |
| NC_000009.11:g.135775735del , CM000671.1:g.135775735del | GRCh37 |
| NC_000009.10:g.134765556del | NCBI36 |
| NG_012386.1:g.49286del , LRG_486:g.49286del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.2622+367del | ENSP00000496126.2:n.2622+367del | |
| ENST00000490179.4:c.2625+367del | ENSP00000495533.2:n.2625+367del | |
| ENST00000642261.2:c.*404+367del | ENSP00000494743.2:n.*404+367del | |
| ENST00000643275.2:c.*565+367del | ENSP00000495598.2:n.*565+367del | |
| ENST00000643362.2:c.2238+367del | ENSP00000496398.2:n.2238+367del | |
| ENST00000643625.2:c.*367+367del | ENSP00000495546.2:n.*367+367del | |
| ENST00000643691.2:c.2262+367del | ENSP00000494916.2:n.2262+367del | |
| ENST00000644184.2:c.2583+367del | ENSP00000495428.2:n.2583+367del | |
| ENST00000645129.2:c.2469+367del | ENSP00000493639.2:n.2469+367del | |
| ENST00000646440.2:c.2625+367del | ENSP00000495830.2:n.2625+367del | |
| ENST00000298552.9:c.2625+367del MANE Select | ENSP00000298552.3:n.2625+367del | |
| ENST00000642261.1:c.685+367del | ||
| ENST00000642617.1:c.2622+367del | ENSP00000493773.1:n.2622+367del | |
| ENST00000642627.1:c.2607+367del | ENSP00000496772.1:n.2607+367del | |
| ENST00000642811.1:c.*2395+367del | ENSP00000495554.1:n.*2395+367del | |
| ENST00000643072.1:c.2472+367del | ENSP00000496691.1:n.2472+367del | |
| ENST00000643275.1:c.1099+367del | ENSP00000495598.1:n.1099+367del | |
| ENST00000643583.1:c.2610+367del | ENSP00000494685.1:n.2610+367del | |
| ENST00000643625.1:c.502+367del | ENSP00000495546.1:n.502+367del | |
| ENST00000643875.1:c.2625+367del | ENSP00000495158.1:n.2625+367del | |
| ENST00000644097.1:c.2622+367del | ENSP00000494682.1:n.2622+367del | |
| ENST00000644184.1:c.1320+367del | ENSP00000495428.1:n.1320+367del | |
| ENST00000644255.1:c.*2392+367del | ENSP00000493608.1:n.*2392+367del | |
| ENST00000644319.1:n.3000+367del | ||
| ENST00000644786.1:n.284+367del | ||
| ENST00000644882.1:n.1538+367del | ||
| ENST00000645901.1:n.3476+367del | ||
| ENST00000646391.1:c.*2395+367del | ENSP00000494104.1:n.*2395+367del | |
| ENST00000646625.1:c.2625+367del | ENSP00000496263.1:n.2625+367del | |
| ENST00000647262.1:n.1590+367del | ||
| ENST00000647279.1:c.*1864+367del | ENSP00000494502.1:n.*1864+367del | |
| ENST00000647506.1:n.3868del | ||
| ENST00000647534.1:n.1689+367del | ||
| ENST00000298552.7:c.2625+367del | ENSP00000298552.3:n.2625+367del | |
| ENST00000440111.6:c.2625+367del | ENSP00000394524.2:n.2625+367del | |
| ENST00000545250.5:c.2472+367del | ENSP00000444017.1:n.2472+367del | |
| NM_000368.4:c.2625+367del , LRG_486t1:c.2625+367del | NP_000359.1:n.2625+367del | |
| NM_001162426.1:c.2622+367del | NP_001155898.1:n.2622+367del | |
| NM_001162427.1:c.2472+367del | NP_001155899.1:n.2472+367del | |
| XM_005272211.1:c.2625+367del | XP_005272268.1:n.2625+367del | |
| XM_006717271.1:c.2625+367del | XP_006717334.1:n.2625+367del | |
| XM_011518979.1:c.2625+367del | XP_011517281.1:n.2625+367del | |
| NM_001362177.1:c.2262+367del | NP_001349106.1:n.2262+367del | |
| XM_011518979.2:c.2625+367del | XP_011517281.1:n.2625+367del | |
| XM_017015096.1:c.2625+367del | XP_016870585.1:n.2625+367del | |
| XM_017015097.1:c.2625+367del | XP_016870586.1:n.2625+367del | |
| XM_017015098.1:c.2622+367del | XP_016870587.1:n.2622+367del | |
| XM_017015100.1:c.2262+367del | XP_016870589.1:n.2262+367del | |
| XM_017015101.1:c.2259+367del | XP_016870590.1:n.2259+367del | |
| NM_000368.5:c.2625+367del MANE Select | NP_000359.1:n.2625+367del | |
| NM_001162426.2:c.2622+367del | NP_001155898.1:n.2622+367del | |
| NM_001162427.2:c.2472+367del | NP_001155899.1:n.2472+367del | |
| NM_001362177.2:c.2262+367del | NP_001349106.1:n.2262+367del |