Linked Data
ClinVar Variation Id:
220763
dbSNP Id:
rs587782554
ExAC:
11:108190736 C / CTT
gnomAD v2:
11-108190736-C-CTT
gnomAD v3:
11-108320009-C-CTT
gnomAD v4:
11-108320009-C-CTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108320010_108320011insTT , CM000673.2:g.108320010_108320011insTT | GRCh38 |
| NC_000011.9:g.108190737_108190738insTT , CM000673.1:g.108190737_108190738insTT | GRCh37 |
| NC_000011.8:g.107695947_107695948insTT | NCBI36 |
| NG_009830.1:g.102179_102180insTT , LRG_135:g.102179_102180insTT | |
| NG_054724.1:g.154823_154824insAA |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000452508.7:c.6404_6405insTT (ATM) | ENSP00000388058.2:p.Arg2136Ter | |
| ENST00000713593.1:c.*5875_*5876insTT (ATM) | ENSP00000518889.1:n.*5875_*5876insTT | |
| ENST00000278616.9:c.6404_6405insTT (ATM) | ENSP00000278616.4:p.Arg2136Ter | |
| ENST00000525056.2:n.823_824insTT (ATM) | ||
| ENST00000682286.1:n.1161_1162insTT (ATM) | ||
| ENST00000682302.1:n.822_823insTT (ATM) | ||
| ENST00000683174.1:n.7888_7889insTT (ATM) | ||
| ENST00000683524.1:n.1628_1629insTT (ATM) | ||
| ENST00000684152.1:n.2118_2119insTT (ATM) | ||
| ENST00000527805.6:c.*1468_*1469insTT (ATM) | ENSP00000435747.2:n.*1468_*1469insTT | |
| ENST00000675595.1:c.*1468_*1469insTT (ATM) | ENSP00000502563.1:n.*1468_*1469insTT | |
| ENST00000675843.1:c.6404_6405insTT (ATM) MANE Select | ENSP00000501606.1:p.Arg2136Ter | |
| ENST00000278616.8:c.6404_6405insTT (ATM) | ENSP00000278616.4:p.Arg2136Ter | |
| ENST00000452508.6:c.6404_6405insTT (ATM) | ENSP00000388058.2:p.Arg2136Ter | |
| ENST00000524792.5:n.2619_2620insTT (ATM) | ||
| ENST00000525729.5:c.641-10939_641-10938insAA (C11orf65) | ENSP00000433395.1:n.641-10939_641-10938in... | |
| ENST00000533690.5:n.1808_1809insTT (ATM) | ||
| NM_000051.3:c.6404_6405insTT , LRG_135t1:c.6404_6405insTT (ATM) | NP_000042.3:p.Arg2136Ter | |
| XM_005271561.3:c.6404_6405insTT (ATM) | XP_005271618.2:p.Arg2136Ter | |
| XM_005271562.3:c.6404_6405insTT (ATM) | XP_005271619.2:p.Arg2136Ter | |
| XM_006718843.2:c.6404_6405insTT (ATM) | XP_006718906.1:p.Arg2136Ter | |
| XM_006718845.1:c.2360_2361insTT (ATM) | XP_006718908.1:p.Arg788Ter | |
| XM_011542840.1:c.6404_6405insTT (ATM) | XP_011541142.1:p.Arg2136Ter | |
| XM_011542841.1:c.6404_6405insTT (ATM) | XP_011541143.1:p.Arg2136Ter | |
| XM_011542842.1:c.6239_6240insTT (ATM) | XP_011541144.1:p.Arg2081Ter | |
| XM_011542843.1:c.6404_6405insTT (ATM) | XP_011541145.1:p.Arg2136Ter | |
| XM_011542844.1:c.5360_5361insTT (ATM) | XP_011541146.1:p.Arg1788Ter | |
| XM_011542845.1:c.5096_5097insTT (ATM) | XP_011541147.1:p.Arg1700Ter | |
| XM_011542847.1:c.1475_1476insTT (ATM) | XP_011541149.1:p.Arg493Ter | |
| NM_001330368.1:c.641-10939_641-10938insAA (C11orf65) | NP_001317297.1:n.641-10939_641-10938insAA... | |
| NM_001351110.1:c.*39-10939_*39-10938insAA (C11orf65) | NP_001338039.1:n.*39-10939_*39-10938insAA... | |
| NM_001351834.1:c.6404_6405insTT (ATM) | NP_001338763.1:p.Arg2136Ter | |
| XM_005271562.5:c.6404_6405insTT (ATM) | XP_005271619.2:p.Arg2136Ter | |
| XM_006718843.4:c.6404_6405insTT (ATM) | XP_006718906.1:p.Arg2136Ter | |
| XM_006718845.2:c.2360_2361insTT (ATM) | XP_006718908.1:p.Arg788Ter | |
| XM_011542840.3:c.6404_6405insTT (ATM) | XP_011541142.1:p.Arg2136Ter | |
| XM_011542842.3:c.6239_6240insTT (ATM) | XP_011541144.1:p.Arg2081Ter | |
| XM_011542843.2:c.6404_6405insTT (ATM) | XP_011541145.1:p.Arg2136Ter | |
| XM_011542844.3:c.5360_5361insTT (ATM) | XP_011541146.1:p.Arg1788Ter | |
| XM_011542845.2:c.5096_5097insTT (ATM) | XP_011541147.1:p.Arg1700Ter | |
| XM_017017789.2:c.6404_6405insTT (ATM) | XP_016873278.1:p.Arg2136Ter | |
| XM_017017790.2:c.6404_6405insTT (ATM) | XP_016873279.1:p.Arg2136Ter | |
| XM_017017791.1:c.6404_6405insTT (ATM) | XP_016873280.1:p.Arg2136Ter | |
| NM_001330368.2:c.641-10939_641-10938insAA (C11orf65) | NP_001317297.1:n.641-10939_641-10938insAA... | |
| NM_001351110.2:c.*39-10939_*39-10938insAA (C11orf65) | NP_001338039.1:n.*39-10939_*39-10938insAA... | |
| NM_001351834.2:c.6404_6405insTT (ATM) | NP_001338763.1:p.Arg2136Ter | |
| NM_000051.4:c.6404_6405insTT (ATM) MANE Select | NP_000042.3:p.Arg2136Ter |