Linked Data
ClinVar Variation Id:
629433
ClinVar RCV Id:
RCV000774140
dbSNP Id:
rs1060504316
MyVariant Identifiers:
chr11:g.108186630C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108315903C>G , CM000673.2:g.108315903C>G | GRCh38 |
| NC_000011.9:g.108186630C>G , CM000673.1:g.108186630C>G | GRCh37 |
| NC_000011.8:g.107691840C>G | NCBI36 |
| NG_009830.1:g.98072C>G , LRG_135:g.98072C>G | |
| NG_054724.1:g.158930G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.6087C>G (ATM) | ENSP00000388058.2:p.Pro2029= | |
| ENST00000713593.1:c.*5558C>G (ATM) | ENSP00000518889.1:n.*5558C>G | |
| ENST00000278616.9:c.6087C>G (ATM) | ENSP00000278616.4:p.Pro2029= | |
| ENST00000525056.2:n.506C>G (ATM) | ||
| ENST00000682286.1:n.844C>G (ATM) | ||
| ENST00000682302.1:n.505C>G (ATM) | ||
| ENST00000683174.1:n.7571C>G (ATM) | ||
| ENST00000683524.1:n.1311C>G (ATM) | ||
| ENST00000684152.1:n.1801C>G (ATM) | ||
| ENST00000527805.6:c.*1151C>G (ATM) | ENSP00000435747.2:n.*1151C>G | |
| ENST00000675595.1:c.*1151C>G (ATM) | ENSP00000502563.1:n.*1151C>G | |
| ENST00000675843.1:c.6087C>G (ATM) MANE Select | ENSP00000501606.1:p.Pro2029= | |
| ENST00000278616.8:c.6087C>G (ATM) | ENSP00000278616.4:p.Pro2029= | |
| ENST00000452508.6:c.6087C>G (ATM) | ENSP00000388058.2:p.Pro2029= | |
| ENST00000524792.5:n.2302C>G (ATM) | ||
| ENST00000525729.5:c.641-6832G>C (C11orf65) | ENSP00000433395.1:n.641-6832G>C | |
| ENST00000532765.1:n.404C>G (ATM) | ||
| ENST00000533690.5:n.1491C>G (ATM) | ||
| NM_000051.3:c.6087C>G , LRG_135t1:c.6087C>G (ATM) | NP_000042.3:p.Pro2029= | |
| XM_005271561.3:c.6087C>G (ATM) | XP_005271618.2:p.Pro2029= | |
| XM_005271562.3:c.6087C>G (ATM) | XP_005271619.2:p.Pro2029= | |
| XM_006718843.2:c.6087C>G (ATM) | XP_006718906.1:p.Pro2029= | |
| XM_006718845.1:c.2043C>G (ATM) | XP_006718908.1:p.Pro681= | |
| XM_011542840.1:c.6087C>G (ATM) | XP_011541142.1:p.Pro2029= | |
| XM_011542841.1:c.6087C>G (ATM) | XP_011541143.1:p.Pro2029= | |
| XM_011542842.1:c.5922C>G (ATM) | XP_011541144.1:p.Pro1974= | |
| XM_011542843.1:c.6087C>G (ATM) | XP_011541145.1:p.Pro2029= | |
| XM_011542844.1:c.5043C>G (ATM) | XP_011541146.1:p.Pro1681= | |
| XM_011542845.1:c.4779C>G (ATM) | XP_011541147.1:p.Pro1593= | |
| XM_011542847.1:c.1158C>G (ATM) | XP_011541149.1:p.Pro386= | |
| NM_001330368.1:c.641-6832G>C (C11orf65) | NP_001317297.1:n.641-6832G>C | |
| NM_001351110.1:c.*39-6832G>C (C11orf65) | NP_001338039.1:n.*39-6832G>C | |
| NM_001351834.1:c.6087C>G (ATM) | NP_001338763.1:p.Pro2029= | |
| XM_005271562.5:c.6087C>G (ATM) | XP_005271619.2:p.Pro2029= | |
| XM_006718843.4:c.6087C>G (ATM) | XP_006718906.1:p.Pro2029= | |
| XM_006718845.2:c.2043C>G (ATM) | XP_006718908.1:p.Pro681= | |
| XM_011542840.3:c.6087C>G (ATM) | XP_011541142.1:p.Pro2029= | |
| XM_011542842.3:c.5922C>G (ATM) | XP_011541144.1:p.Pro1974= | |
| XM_011542843.2:c.6087C>G (ATM) | XP_011541145.1:p.Pro2029= | |
| XM_011542844.3:c.5043C>G (ATM) | XP_011541146.1:p.Pro1681= | |
| XM_011542845.2:c.4779C>G (ATM) | XP_011541147.1:p.Pro1593= | |
| XM_017017789.2:c.6087C>G (ATM) | XP_016873278.1:p.Pro2029= | |
| XM_017017790.2:c.6087C>G (ATM) | XP_016873279.1:p.Pro2029= | |
| XM_017017791.1:c.6087C>G (ATM) | XP_016873280.1:p.Pro2029= | |
| NM_001330368.2:c.641-6832G>C (C11orf65) | NP_001317297.1:n.641-6832G>C | |
| NM_001351110.2:c.*39-6832G>C (C11orf65) | NP_001338039.1:n.*39-6832G>C | |
| NM_001351834.2:c.6087C>G (ATM) | NP_001338763.1:p.Pro2029= | |
| NM_000051.4:c.6087C>G (ATM) MANE Select | NP_000042.3:p.Pro2029= |