Linked Data
dbSNP Id:
rs1357479850
gnomAD v2:
5-161581136-TG-T
gnomAD v3:
5-162154130-TG-T
gnomAD v4:
5-162154130-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.162154131del , CM000667.2:g.162154131del | GRCh38 |
| NC_000005.9:g.161581137del , CM000667.1:g.161581137del | GRCh37 |
| NC_000005.8:g.161513715del | NCBI36 |
| NG_009290.1:g.91490del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356592.8:c.2192del | ||
| ENST00000361925.9:c.*763del | ENSP00000354651.5:n.*763del | |
| ENST00000638552.1:c.*763del | ENSP00000491763.1:n.*763del | |
| ENST00000638660.1:c.*763del | ENSP00000492869.1:n.*763del | |
| ENST00000638772.1:c.*4788del | ENSP00000491557.1:n.*4788del | |
| ENST00000638877.1:c.2068del | ||
| ENST00000639046.1:c.*763del | ENSP00000492659.1:n.*763del | |
| ENST00000639111.2:c.*763del | ENSP00000492125.2:n.*763del | |
| ENST00000639213.2:c.*763del MANE Select | ENSP00000491909.2:n.*763del | |
| ENST00000639278.1:c.2854del | ENSP00000491958.1:n.2854del | |
| ENST00000639384.1:c.*2372del | ENSP00000491240.1:n.*2372del | |
| ENST00000639424.1:c.*1391del | ENSP00000491245.1:n.*1391del | |
| ENST00000639683.1:c.*763del | ENSP00000492581.1:n.*763del | |
| ENST00000639975.1:c.*763del | ENSP00000492096.1:n.*763del | |
| ENST00000640500.1:n.1465del | ||
| ENST00000640739.1:n.7138del | ||
| ENST00000640985.1:c.*763del | ENSP00000492293.1:n.*763del | |
| ENST00000641017.1:c.2260del | ENSP00000493461.1:n.2260del | |
| ENST00000356592.7:c.*763del | ENSP00000349000.3:n.*763del | |
| ENST00000414552.6:c.*763del | ENSP00000410732.2:n.*763del | |
| NM_000816.3:c.*763del | NP_000807.2:n.*763del | |
| NM_198903.2:c.*763del | NP_944493.2:n.*763del | |
| NM_198904.2:c.*763del | NP_944494.1:n.*763del | |
| NM_001375339.1:c.*763del | NP_001362268.1:n.*763del | |
| NM_001375340.1:c.*1025del | NP_001362269.1:n.*1025del | |
| NM_001375341.1:c.*763del | NP_001362270.1:n.*763del | |
| NM_001375342.1:c.*763del | NP_001362271.1:n.*763del | |
| NM_001375343.1:c.*763del | NP_001362272.1:n.*763del | |
| NM_001375344.1:c.*763del | NP_001362273.1:n.*763del | |
| NM_001375345.1:c.*763del | NP_001362274.1:n.*763del | |
| NM_001375346.1:c.*763del | NP_001362275.1:n.*763del | |
| NM_001375347.1:c.*763del | NP_001362276.1:n.*763del | |
| NM_001375348.1:c.*763del | NP_001362277.1:n.*763del | |
| NM_001375349.1:c.*763del | NP_001362278.1:n.*763del | |
| NM_001375350.1:c.*763del | NP_001362279.1:n.*763del | |
| NM_198904.3:c.*763del | NP_944494.1:n.*763del | |
| NM_198904.4:c.*763del MANE Select | NP_944494.1:n.*763del |