Linked Data
ClinVar Variation Id:
319676
ClinVar RCV Id:
RCV000296143
dbSNP Id:
rs141907159
ExAC:
16:53738092 GC / G
gnomAD v2:
16-53738092-GC-G
gnomAD v3:
16-53704180-GC-G
gnomAD v4:
16-53704180-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.53704181del , CM000678.2:g.53704181del | GRCh38 |
| NC_000016.9:g.53738093del , CM000678.1:g.53738093del | GRCh37 |
| NC_000016.8:g.52295594del | NCBI36 |
| NG_008991.2:g.4679del | |
| NG_012969.1:g.5219del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000471389.6:c.-4del MANE Select | ENSP00000418823.1:n.-4del | |
| ENST00000636030.1:n.24del | ||
| ENST00000636218.1:c.-4del | ENSP00000489641.1:n.-4del | |
| ENST00000636491.1:c.-68+2360del | ENSP00000490047.1:n.-68+2360del | |
| ENST00000636992.1:c.-4del | ENSP00000489886.1:n.-4del | |
| ENST00000637001.1:c.-4del | ENSP00000489936.1:n.-4del | |
| ENST00000637562.1:c.-4del | ENSP00000490426.1:n.-4del | |
| ENST00000637845.1:c.-4del | ENSP00000489638.1:n.-4del | |
| ENST00000637969.1:c.-4del | ENSP00000490516.1:n.-4del | |
| ENST00000471389.5:c.-4del | ENSP00000418823.1:n.-4del | |
| ENST00000570395.1:n.26del | ||
| NM_001080432.2:c.-4del | NP_001073901.1:n.-4del | |
| XM_011523313.1:c.-4del | XP_011521615.1:n.-4del | |
| XM_011523314.1:c.-4del | XP_011521616.1:n.-4del | |
| XM_011523315.1:c.-4del | XP_011521617.1:n.-4del | |
| XM_011523316.1:c.-4del | XP_011521618.1:n.-4del | |
| NM_001363891.1:c.-4del | NP_001350820.1:n.-4del | |
| NM_001363894.1:c.-4del | NP_001350823.1:n.-4del | |
| NM_001363896.1:c.-4del | NP_001350825.1:n.-4del | |
| NM_001363897.1:c.-4del | NP_001350826.1:n.-4del | |
| NM_001363898.1:c.-4del | NP_001350827.1:n.-4del | |
| NM_001363899.1:c.-4del | NP_001350828.1:n.-4del | |
| NM_001363900.1:c.-4del | NP_001350829.1:n.-4del | |
| NM_001363901.1:c.-4del | NP_001350830.1:n.-4del | |
| NM_001363903.1:c.-4del | NP_001350832.1:n.-4del | |
| NM_001363905.1:c.-696del | NP_001350834.1:n.-696del | |
| NM_001363988.1:c.-4del | NP_001350917.1:n.-4del | |
| NR_156761.1:n.219del | ||
| XM_011523314.3:c.-4del | XP_011521616.1:n.-4del | |
| XM_011523315.3:c.-4del | XP_011521617.1:n.-4del | |
| XM_011523316.3:c.-4del | XP_011521618.1:n.-4del | |
| XM_017023654.2:c.-4del | XP_016879143.1:n.-4del | |
| XM_017023655.2:c.-4del | XP_016879144.1:n.-4del | |
| XM_017023656.2:c.-4del | XP_016879145.1:n.-4del | |
| XM_017023657.2:c.-4del | XP_016879146.1:n.-4del | |
| XM_017023658.2:c.-4del | XP_016879147.1:n.-4del | |
| XM_024450437.1:c.-4del | XP_024306205.1:n.-4del | |
| XR_002957840.1:n.40del | ||
| NM_001080432.3:c.-4del MANE Select | NP_001073901.1:n.-4del |