Linked Data
dbSNP Id:
rs1333930817
gnomAD v2:
14-65569149-T-TC
gnomAD v3:
14-65102431-T-TC
gnomAD v4:
14-65102431-T-TC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65102438dup , CM000676.2:g.65102438dup | GRCh38 |
| NC_000014.8:g.65569156dup , CM000676.1:g.65569156dup | GRCh37 |
| NC_000014.7:g.64638909dup | NCBI36 |
| NG_029830.1:g.5078dup , LRG_530:g.5078dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000556892.6:c.-157+77dup | ENSP00000452206.2:n.-157+77dup | |
| ENST00000556979.6:c.-93dup | ENSP00000452378.1:n.-93dup | |
| ENST00000358664.9:c.-93dup MANE Select | ENSP00000351490.4:n.-93dup | |
| ENST00000246163.2:c.-93dup | ENSP00000246163.2:n.-93dup | |
| ENST00000284165.10:c.-93dup | ENSP00000284165.6:n.-93dup | |
| ENST00000358402.8:c.-93dup | ENSP00000351175.4:n.-93dup | |
| ENST00000358664.8:c.-93dup | ENSP00000351490.4:n.-93dup | |
| ENST00000394606.6:c.-93dup | ENSP00000378104.2:n.-93dup | |
| ENST00000554709.1:n.86dup | ||
| ENST00000555667.5:c.-93dup | ENSP00000452286.1:n.-93dup | |
| ENST00000555932.5:c.-93dup | ENSP00000450763.1:n.-93dup | |
| ENST00000556443.5:c.-93dup | ENSP00000450818.1:n.-93dup | |
| ENST00000556702.1:n.47dup | ||
| ENST00000556892.5:c.-157+77dup | ENSP00000452206.1:n.-157+77dup | |
| ENST00000556979.5:c.-93dup | ENSP00000452378.1:n.-93dup | |
| ENST00000557277.5:c.-239+77dup | ENSP00000450955.1:n.-239+77dup | |
| ENST00000557746.5:c.-93dup | ENSP00000452197.1:n.-93dup | |
| ENST00000618858.4:c.-93dup | ENSP00000480127.1:n.-93dup | |
| NM_001271068.1:c.-93dup | NP_001257997.1:n.-93dup | |
| NM_001271069.1:c.-93dup | NP_001257998.1:n.-93dup | |
| NM_002382.4:c.-93dup | NP_002373.3:n.-93dup | |
| NM_145112.2:c.-93dup | NP_660087.1:n.-93dup | |
| NM_145113.2:c.-93dup | NP_660088.1:n.-93dup | |
| NM_145114.2:c.-93dup | NP_660089.1:n.-93dup | |
| NM_197957.3:c.-93dup | NP_932061.1:n.-93dup | |
| NR_073137.1:n.187+77dup | ||
| NR_073138.1:n.187+77dup | ||
| XM_011536773.1:c.-93dup | XP_011535075.1:n.-93dup | |
| XR_429315.2:n.110dup | ||
| XR_943450.1:n.110dup | ||
| XR_943451.1:n.110dup | ||
| XR_943452.1:n.99dup | ||
| NM_001320415.1:c.-367dup | NP_001307344.1:n.-367dup | |
| XM_011536773.3:c.-93dup | XP_011535075.1:n.-93dup | |
| XM_017021312.2:c.-340dup | XP_016876801.1:n.-340dup | |
| XR_001750326.2:n.98dup | ||
| XR_001750327.2:n.98dup | ||
| XR_002957553.1:n.101dup | ||
| XR_943450.3:n.110dup | ||
| XR_943451.3:n.110dup | ||
| XR_943452.3:n.98dup | ||
| NM_001320415.2:c.-367dup | NP_001307344.1:n.-367dup | |
| NM_002382.5:c.-93dup MANE Select | NP_002373.3:n.-93dup | |
| NM_145112.3:c.-93dup | NP_660087.1:n.-93dup | |
| NM_145113.3:c.-93dup | NP_660088.1:n.-93dup | |
| NM_001271068.2:c.-93dup | NP_001257997.1:n.-93dup | |
| NM_001271069.2:c.-93dup | NP_001257998.1:n.-93dup | |
| NM_145114.3:c.-93dup | NP_660089.1:n.-93dup | |
| NM_197957.4:c.-93dup | NP_932061.1:n.-93dup |