Linked Data
ClinVar Variation Id:
135780
ClinVar RCV Id:
RCV000122886
RCV000128904
RCV000212082
RCV001356913
RCV002483233
RCV002272133
RCV003492532
dbSNP Id:
rs371638537
ExAC:
11:108206686 A / T
gnomAD v2:
11-108206686-A-T
gnomAD v3:
11-108335959-A-T
gnomAD v4:
11-108335959-A-T
COSMIC:
COSM758333
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108335959A>T , CM000673.2:g.108335959A>T | GRCh38 |
| NC_000011.9:g.108206686A>T , CM000673.1:g.108206686A>T | GRCh37 |
| NC_000011.8:g.107711896A>T | NCBI36 |
| NG_009830.1:g.118128A>T , LRG_135:g.118128A>T | |
| NG_054724.1:g.138874T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8266A>T (ATM) | ENSP00000388058.2:p.Lys2756Ter | |
| ENST00000713593.1:c.*7737A>T (ATM) | ENSP00000518889.1:n.*7737A>T | |
| ENST00000278616.9:c.8266A>T (ATM) | ENSP00000278616.4:p.Lys2756Ter | |
| ENST00000525056.2:n.2685A>T (ATM) | ||
| ENST00000638786.2:n.964A>T (ATM) | ||
| ENST00000682286.1:n.3023A>T (ATM) | ||
| ENST00000682302.1:n.2684A>T (ATM) | ||
| ENST00000683174.1:n.9750A>T (ATM) | ||
| ENST00000683524.1:n.3490A>T (ATM) | ||
| ENST00000684152.1:n.3682A>T (ATM) | ||
| ENST00000684180.1:n.740A>T (ATM) | ||
| ENST00000684447.1:n.4759A>T (ATM) | ||
| ENST00000527805.6:c.*3330A>T (ATM) | ENSP00000435747.2:n.*3330A>T | |
| ENST00000675595.1:c.*3401A>T (ATM) | ENSP00000502563.1:n.*3401A>T | |
| ENST00000675843.1:c.8266A>T (ATM) MANE Select | ENSP00000501606.1:p.Lys2756Ter | |
| ENST00000278616.8:c.8266A>T (ATM) | ENSP00000278616.4:p.Lys2756Ter | |
| ENST00000452508.6:c.8266A>T (ATM) | ENSP00000388058.2:p.Lys2756Ter | |
| ENST00000524755.5:c.227-667T>A (C11orf65) | ||
| ENST00000524792.5:n.4481A>T (ATM) | ||
| ENST00000525056.1:n.463A>T (ATM) | ||
| ENST00000525729.5:c.641-26888T>A (C11orf65) | ENSP00000433395.1:n.641-26888T>A | |
| ENST00000527531.5:c.*1197-667T>A (C11orf65) | ENSP00000431706.1:n.*1197-667T>A | |
| ENST00000533979.5:n.478A>T (ATM) | ||
| ENST00000615746.4:c.*1197-667T>A (C11orf65) | ENSP00000483537.1:n.*1197-667T>A | |
| NM_000051.3:c.8266A>T , LRG_135t1:c.8266A>T (ATM) | NP_000042.3:p.Lys2756Ter | |
| XM_005271414.3:c.788-667T>A (C11orf65) | XP_005271471.1:n.788-667T>A | |
| XM_005271415.3:c.732-667T>A (C11orf65) | XP_005271472.1:n.732-667T>A | |
| XM_005271561.3:c.8266A>T (ATM) | XP_005271618.2:p.Lys2756Ter | |
| XM_005271562.3:c.8266A>T (ATM) | XP_005271619.2:p.Lys2756Ter | |
| XM_006718843.2:c.8266A>T (ATM) | XP_006718906.1:p.Lys2756Ter | |
| XM_006718845.1:c.4222A>T (ATM) | XP_006718908.1:p.Lys1408Ter | |
| XM_011542840.1:c.8266A>T (ATM) | XP_011541142.1:p.Lys2756Ter | |
| XM_011542841.1:c.8266A>T (ATM) | XP_011541143.1:p.Lys2756Ter | |
| XM_011542842.1:c.8101A>T (ATM) | XP_011541144.1:p.Lys2701Ter | |
| XM_011542843.1:c.8266A>T (ATM) | XP_011541145.1:p.Lys2756Ter | |
| XM_011542844.1:c.7222A>T (ATM) | XP_011541146.1:p.Lys2408Ter | |
| XM_011542845.1:c.6958A>T (ATM) | XP_011541147.1:p.Lys2320Ter | |
| XM_011542847.1:c.3337A>T (ATM) | XP_011541149.1:p.Lys1113Ter | |
| NM_001330368.1:c.641-26888T>A (C11orf65) | NP_001317297.1:n.641-26888T>A | |
| NM_001351110.1:c.695-667T>A (C11orf65) | NP_001338039.1:n.695-667T>A | |
| NM_001351834.1:c.8266A>T (ATM) | NP_001338763.1:p.Lys2756Ter | |
| NR_147053.2:n.2302-667T>A (C11orf65) | ||
| XM_005271414.4:c.788-667T>A (C11orf65) | XP_005271471.1:n.788-667T>A | |
| XM_005271415.4:c.732-667T>A (C11orf65) | XP_005271472.1:n.732-667T>A | |
| XM_005271562.5:c.8266A>T (ATM) | XP_005271619.2:p.Lys2756Ter | |
| XM_006718843.4:c.8266A>T (ATM) | XP_006718906.1:p.Lys2756Ter | |
| XM_006718845.2:c.4222A>T (ATM) | XP_006718908.1:p.Lys1408Ter | |
| XM_011542840.3:c.8266A>T (ATM) | XP_011541142.1:p.Lys2756Ter | |
| XM_011542842.3:c.8101A>T (ATM) | XP_011541144.1:p.Lys2701Ter | |
| XM_011542843.2:c.8266A>T (ATM) | XP_011541145.1:p.Lys2756Ter | |
| XM_011542844.3:c.7222A>T (ATM) | XP_011541146.1:p.Lys2408Ter | |
| XM_011542845.2:c.6958A>T (ATM) | XP_011541147.1:p.Lys2320Ter | |
| XM_017017789.2:c.8266A>T (ATM) | XP_016873278.1:p.Lys2756Ter | |
| XM_017017790.2:c.8266A>T (ATM) | XP_016873279.1:p.Lys2756Ter | |
| NM_001330368.2:c.641-26888T>A (C11orf65) | NP_001317297.1:n.641-26888T>A | |
| NM_001351110.2:c.695-667T>A (C11orf65) | NP_001338039.1:n.695-667T>A | |
| NM_001351834.2:c.8266A>T (ATM) | NP_001338763.1:p.Lys2756Ter | |
| NM_000051.4:c.8266A>T (ATM) MANE Select | NP_000042.3:p.Lys2756Ter | |
| NR_147053.3:n.2300-667T>A (C11orf65) |