Linked Data
dbSNP Id:
rs761729566
ExAC:
11:108154916 TTATA / T
gnomAD v2:
11-108154916-TTATA-T
gnomAD v4:
11-108284189-TTATA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108284194_108284197del , CM000673.2:g.108284194_108284197del | GRCh38 |
| NC_000011.9:g.108154921_108154924del , CM000673.1:g.108154921_108154924del | GRCh37 |
| NC_000011.8:g.107660131_107660134del | NCBI36 |
| NG_009830.1:g.66363_66366del , LRG_135:g.66363_66366del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000452508.7:c.3747-33_3747-30del | ENSP00000388058.2:n.3747-33_3747-30del | |
| ENST00000713593.1:c.*3218-33_*3218-30del | ENSP00000518889.1:n.*3218-33_*3218-30del | |
| ENST00000278616.9:c.3747-33_3747-30del | ENSP00000278616.4:n.3747-33_3747-30del | |
| ENST00000682289.1:n.94-33_94-30del | ||
| ENST00000683174.1:n.3897-33_3897-30del | ||
| ENST00000527805.6:c.3747-33_3747-30del | ENSP00000435747.2:n.3747-33_3747-30del | |
| ENST00000675595.1:c.3582-33_3582-30del | ENSP00000502563.1:n.3582-33_3582-30del | |
| ENST00000675843.1:c.3747-33_3747-30del MANE Select | ENSP00000501606.1:n.3747-33_3747-30del | |
| ENST00000278616.8:c.3747-33_3747-30del | ENSP00000278616.4:n.3747-33_3747-30del | |
| ENST00000452508.6:c.3747-33_3747-30del | ENSP00000388058.2:n.3747-33_3747-30del | |
| ENST00000527805.5:c.3747-33_3747-30del | ENSP00000435747.1:n.3747-33_3747-30del | |
| NM_000051.3:c.3747-33_3747-30del , LRG_135t1:c.3747-33_3747-30del | NP_000042.3:n.3747-33_3747-30del | |
| XM_005271561.3:c.3747-33_3747-30del | XP_005271618.2:n.3747-33_3747-30del | |
| XM_005271562.3:c.3747-33_3747-30del | XP_005271619.2:n.3747-33_3747-30del | |
| XM_006718843.2:c.3747-33_3747-30del | XP_006718906.1:n.3747-33_3747-30del | |
| XM_011542840.1:c.3747-33_3747-30del | XP_011541142.1:n.3747-33_3747-30del | |
| XM_011542841.1:c.3747-33_3747-30del | XP_011541143.1:n.3747-33_3747-30del | |
| XM_011542842.1:c.3582-33_3582-30del | XP_011541144.1:n.3582-33_3582-30del | |
| XM_011542843.1:c.3747-33_3747-30del | XP_011541145.1:n.3747-33_3747-30del | |
| XM_011542844.1:c.2703-33_2703-30del | XP_011541146.1:n.2703-33_2703-30del | |
| XM_011542845.1:c.2439-33_2439-30del | XP_011541147.1:n.2439-33_2439-30del | |
| XM_011542846.1:c.3747-33_3747-30del | XP_011541148.1:n.3747-33_3747-30del | |
| NM_001351834.1:c.3747-33_3747-30del | NP_001338763.1:n.3747-33_3747-30del | |
| XM_005271562.5:c.3747-33_3747-30del | XP_005271619.2:n.3747-33_3747-30del | |
| XM_006718843.4:c.3747-33_3747-30del | XP_006718906.1:n.3747-33_3747-30del | |
| XM_011542840.3:c.3747-33_3747-30del | XP_011541142.1:n.3747-33_3747-30del | |
| XM_011542842.3:c.3582-33_3582-30del | XP_011541144.1:n.3582-33_3582-30del | |
| XM_011542843.2:c.3747-33_3747-30del | XP_011541145.1:n.3747-33_3747-30del | |
| XM_011542844.3:c.2703-33_2703-30del | XP_011541146.1:n.2703-33_2703-30del | |
| XM_011542845.2:c.2439-33_2439-30del | XP_011541147.1:n.2439-33_2439-30del | |
| XM_017017789.2:c.3747-33_3747-30del | XP_016873278.1:n.3747-33_3747-30del | |
| XM_017017790.2:c.3747-33_3747-30del | XP_016873279.1:n.3747-33_3747-30del | |
| XM_017017791.1:c.3747-33_3747-30del | XP_016873280.1:n.3747-33_3747-30del | |
| XM_017017792.2:c.3747-33_3747-30del | XP_016873281.1:n.3747-33_3747-30del | |
| XR_002957150.1:n.4480-33_4480-30del | ||
| NM_001351834.2:c.3747-33_3747-30del | NP_001338763.1:n.3747-33_3747-30del | |
| NM_000051.4:c.3747-33_3747-30del MANE Select | NP_000042.3:n.3747-33_3747-30del |