Linked Data
ClinVar Variation Id:
133638
ClinVar RCV Id:
RCV000120163
RCV000462707
RCV000764951
RCV000159755
RCV000656764
RCV001798380
RCV003153383
RCV003153384
dbSNP Id:
rs529296539
ExAC:
11:108216546 G / A
gnomAD v2:
11-108216546-G-A
gnomAD v3:
11-108345819-G-A
gnomAD v4:
11-108345819-G-A
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108345819G>A , CM000673.2:g.108345819G>A | GRCh38 |
| NC_000011.9:g.108216546G>A , CM000673.1:g.108216546G>A | GRCh37 |
| NC_000011.8:g.107721756G>A | NCBI36 |
| NG_009830.1:g.127988G>A , LRG_135:g.127988G>A | |
| NG_054724.1:g.129014C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8495G>A (ATM) | ENSP00000388058.2:p.Arg2832His | |
| ENST00000713593.1:c.*7966G>A (ATM) | ENSP00000518889.1:n.*7966G>A | |
| ENST00000278616.9:c.8495G>A (ATM) | ENSP00000278616.4:p.Arg2832His | |
| ENST00000638786.2:n.1193G>A (ATM) | ||
| ENST00000682286.1:n.3252G>A (ATM) | ||
| ENST00000682302.1:n.2913G>A (ATM) | ||
| ENST00000683174.1:n.9979G>A (ATM) | ||
| ENST00000683524.1:n.3719G>A (ATM) | ||
| ENST00000684152.1:n.3911G>A (ATM) | ||
| ENST00000684180.1:n.969G>A (ATM) | ||
| ENST00000684447.1:n.4988G>A (ATM) | ||
| ENST00000527805.6:c.*3559G>A (ATM) | ENSP00000435747.2:n.*3559G>A | |
| ENST00000675595.1:c.*3630G>A (ATM) | ENSP00000502563.1:n.*3630G>A | |
| ENST00000675843.1:c.8495G>A (ATM) MANE Select | ENSP00000501606.1:p.Arg2832His | |
| ENST00000278616.8:c.8495G>A (ATM) | ENSP00000278616.4:p.Arg2832His | |
| ENST00000452508.6:c.8495G>A (ATM) | ENSP00000388058.2:p.Arg2832His | |
| ENST00000524755.5:c.227-10527C>T (C11orf65) | ||
| ENST00000524792.5:n.4710G>A (ATM) | ||
| ENST00000525729.5:c.641-36748C>T (C11orf65) | ENSP00000433395.1:n.641-36748C>T | |
| ENST00000526725.1:n.272-5455C>T (C11orf65) | ||
| ENST00000527531.5:c.*1196+9096C>T (C11orf65) | ENSP00000431706.1:n.*1196+9096C>T | |
| ENST00000615746.4:c.*1196+9096C>T (C11orf65) | ENSP00000483537.1:n.*1196+9096C>T | |
| NM_000051.3:c.8495G>A , LRG_135t1:c.8495G>A (ATM) | NP_000042.3:p.Arg2832His | |
| XM_005271414.3:c.788-10527C>T (C11orf65) | XP_005271471.1:n.788-10527C>T | |
| XM_005271415.3:c.732-10527C>T (C11orf65) | XP_005271472.1:n.732-10527C>T | |
| XM_005271561.3:c.8495G>A (ATM) | XP_005271618.2:p.Arg2832His | |
| XM_005271562.3:c.8495G>A (ATM) | XP_005271619.2:p.Arg2832His | |
| XM_006718843.2:c.8495G>A (ATM) | XP_006718906.1:p.Arg2832His | |
| XM_006718845.1:c.4451G>A (ATM) | XP_006718908.1:p.Arg1484His | |
| XM_011542640.1:c.788-5455C>T (C11orf65) | XP_011540942.1:n.788-5455C>T | |
| XM_011542643.1:c.732-5455C>T (C11orf65) | XP_011540945.1:n.732-5455C>T | |
| XM_011542840.1:c.8495G>A (ATM) | XP_011541142.1:p.Arg2832His | |
| XM_011542841.1:c.8495G>A (ATM) | XP_011541143.1:p.Arg2832His | |
| XM_011542842.1:c.8330G>A (ATM) | XP_011541144.1:p.Arg2777His | |
| XM_011542843.1:c.8495G>A (ATM) | XP_011541145.1:p.Arg2832His | |
| XM_011542844.1:c.7451G>A (ATM) | XP_011541146.1:p.Arg2484His | |
| XM_011542845.1:c.7187G>A (ATM) | XP_011541147.1:p.Arg2396His | |
| XM_011542847.1:c.3566G>A (ATM) | XP_011541149.1:p.Arg1189His | |
| NM_001330368.1:c.641-36748C>T (C11orf65) | NP_001317297.1:n.641-36748C>T | |
| NM_001351110.1:c.695-10527C>T (C11orf65) | NP_001338039.1:n.695-10527C>T | |
| NM_001351834.1:c.8495G>A (ATM) | NP_001338763.1:p.Arg2832His | |
| NR_147053.2:n.2301+9096C>T (C11orf65) | ||
| XM_005271414.4:c.788-10527C>T (C11orf65) | XP_005271471.1:n.788-10527C>T | |
| XM_005271415.4:c.732-10527C>T (C11orf65) | XP_005271472.1:n.732-10527C>T | |
| XM_005271562.5:c.8495G>A (ATM) | XP_005271619.2:p.Arg2832His | |
| XM_006718843.4:c.8495G>A (ATM) | XP_006718906.1:p.Arg2832His | |
| XM_006718845.2:c.4451G>A (ATM) | XP_006718908.1:p.Arg1484His | |
| XM_011542640.2:c.788-5455C>T (C11orf65) | XP_011540942.1:n.788-5455C>T | |
| XM_011542643.2:c.732-5455C>T (C11orf65) | XP_011540945.1:n.732-5455C>T | |
| XM_011542840.3:c.8495G>A (ATM) | XP_011541142.1:p.Arg2832His | |
| XM_011542842.3:c.8330G>A (ATM) | XP_011541144.1:p.Arg2777His | |
| XM_011542843.2:c.8495G>A (ATM) | XP_011541145.1:p.Arg2832His | |
| XM_011542844.3:c.7451G>A (ATM) | XP_011541146.1:p.Arg2484His | |
| XM_011542845.2:c.7187G>A (ATM) | XP_011541147.1:p.Arg2396His | |
| XM_017017247.1:c.904-5455C>T (C11orf65) | XP_016872736.1:n.904-5455C>T | |
| XM_017017789.2:c.8495G>A (ATM) | XP_016873278.1:p.Arg2832His | |
| XM_017017790.2:c.8495G>A (ATM) | XP_016873279.1:p.Arg2832His | |
| NM_001330368.2:c.641-36748C>T (C11orf65) | NP_001317297.1:n.641-36748C>T | |
| NM_001351110.2:c.695-10527C>T (C11orf65) | NP_001338039.1:n.695-10527C>T | |
| NM_001351834.2:c.8495G>A (ATM) | NP_001338763.1:p.Arg2832His | |
| NM_000051.4:c.8495G>A (ATM) MANE Select | NP_000042.3:p.Arg2832His | |
| NR_147053.3:n.2299+9096C>T (C11orf65) |