Linked Data
dbSNP Id:
rs773699157
ExAC:
15:45003856 CT / C
gnomAD v2:
15-45003856-CT-C
gnomAD v3:
15-44711658-CT-C
gnomAD v4:
15-44711658-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44711659del , CM000677.2:g.44711659del | GRCh38 |
| NC_000015.9:g.45003857del , CM000677.1:g.45003857del | GRCh37 |
| NC_000015.8:g.42791149del | NCBI36 |
| NG_012920.1:g.5173del | |
| NG_012920.2:g.5183del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695792.1:n.83+219del | ||
| ENST00000648006.3:c.67+46del MANE Select | ENSP00000497910.1:n.67+46del | |
| ENST00000349264.10:c.57+56del | ENSP00000340858.6:n.57+56del | |
| ENST00000544417.5:c.67+46del | ENSP00000437604.2:n.67+46del | |
| ENST00000557901.5:c.67+46del | ENSP00000452861.1:n.67+46del | |
| ENST00000558401.5:c.67+46del | ENSP00000452780.1:n.67+46del | |
| ENST00000559720.5:n.127+46del | ||
| ENST00000559916.1:c.67+46del | ENSP00000453350.1:n.67+46del | |
| ENST00000561424.5:c.67+46del | ENSP00000453191.1:n.67+46del | |
| NM_004048.2:c.67+46del | NP_004039.1:n.67+46del | |
| XM_005254549.2:c.67+46del | XP_005254606.1:n.67+46del | |
| NM_004048.3:c.67+46del | NP_004039.1:n.67+46del | |
| XM_005254549.3:c.67+46del | XP_005254606.1:n.67+46del | |
| XR_002957658.1:n.122+46del | ||
| NM_004048.4:c.67+46del MANE Select | NP_004039.1:n.67+46del |