Linked Data
ClinVar Variation Id:
921951
dbSNP Id:
rs745709682
MyVariant Identifiers:
chr11:g.108196140C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108325413C>T , CM000673.2:g.108325413C>T | GRCh38 |
| NC_000011.9:g.108196140C>T , CM000673.1:g.108196140C>T | GRCh37 |
| NC_000011.8:g.107701350C>T | NCBI36 |
| NG_009830.1:g.107582C>T , LRG_135:g.107582C>T | |
| NG_054724.1:g.149420G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.6676C>T (ATM) | ENSP00000388058.2:p.Leu2226= | |
| ENST00000713593.1:c.*6147C>T (ATM) | ENSP00000518889.1:n.*6147C>T | |
| ENST00000278616.9:c.6676C>T (ATM) | ENSP00000278616.4:p.Leu2226= | |
| ENST00000525056.2:n.1095C>T (ATM) | ||
| ENST00000682286.1:n.1433C>T (ATM) | ||
| ENST00000682302.1:n.1094C>T (ATM) | ||
| ENST00000683174.1:n.8160C>T (ATM) | ||
| ENST00000683524.1:n.1900C>T (ATM) | ||
| ENST00000684152.1:n.2390C>T (ATM) | ||
| ENST00000527805.6:c.*1740C>T (ATM) | ENSP00000435747.2:n.*1740C>T | |
| ENST00000675595.1:c.*1811C>T (ATM) | ENSP00000502563.1:n.*1811C>T | |
| ENST00000675843.1:c.6676C>T (ATM) MANE Select | ENSP00000501606.1:p.Leu2226= | |
| ENST00000278616.8:c.6676C>T (ATM) | ENSP00000278616.4:p.Leu2226= | |
| ENST00000452508.6:c.6676C>T (ATM) | ENSP00000388058.2:p.Leu2226= | |
| ENST00000524792.5:n.2891C>T (ATM) | ||
| ENST00000525729.5:c.641-16342G>A (C11orf65) | ENSP00000433395.1:n.641-16342G>A | |
| ENST00000533690.5:n.2080C>T (ATM) | ||
| NM_000051.3:c.6676C>T , LRG_135t1:c.6676C>T (ATM) | NP_000042.3:p.Leu2226= | |
| XM_005271561.3:c.6676C>T (ATM) | XP_005271618.2:p.Leu2226= | |
| XM_005271562.3:c.6676C>T (ATM) | XP_005271619.2:p.Leu2226= | |
| XM_006718843.2:c.6676C>T (ATM) | XP_006718906.1:p.Leu2226= | |
| XM_006718845.1:c.2632C>T (ATM) | XP_006718908.1:p.Leu878= | |
| XM_011542840.1:c.6676C>T (ATM) | XP_011541142.1:p.Leu2226= | |
| XM_011542841.1:c.6676C>T (ATM) | XP_011541143.1:p.Leu2226= | |
| XM_011542842.1:c.6511C>T (ATM) | XP_011541144.1:p.Leu2171= | |
| XM_011542843.1:c.6676C>T (ATM) | XP_011541145.1:p.Leu2226= | |
| XM_011542844.1:c.5632C>T (ATM) | XP_011541146.1:p.Leu1878= | |
| XM_011542845.1:c.5368C>T (ATM) | XP_011541147.1:p.Leu1790= | |
| XM_011542847.1:c.1747C>T (ATM) | XP_011541149.1:p.Leu583= | |
| NM_001330368.1:c.641-16342G>A (C11orf65) | NP_001317297.1:n.641-16342G>A | |
| NM_001351110.1:c.*38+9807G>A (C11orf65) | NP_001338039.1:n.*38+9807G>A | |
| NM_001351834.1:c.6676C>T (ATM) | NP_001338763.1:p.Leu2226= | |
| XM_005271562.5:c.6676C>T (ATM) | XP_005271619.2:p.Leu2226= | |
| XM_006718843.4:c.6676C>T (ATM) | XP_006718906.1:p.Leu2226= | |
| XM_006718845.2:c.2632C>T (ATM) | XP_006718908.1:p.Leu878= | |
| XM_011542840.3:c.6676C>T (ATM) | XP_011541142.1:p.Leu2226= | |
| XM_011542842.3:c.6511C>T (ATM) | XP_011541144.1:p.Leu2171= | |
| XM_011542843.2:c.6676C>T (ATM) | XP_011541145.1:p.Leu2226= | |
| XM_011542844.3:c.5632C>T (ATM) | XP_011541146.1:p.Leu1878= | |
| XM_011542845.2:c.5368C>T (ATM) | XP_011541147.1:p.Leu1790= | |
| XM_017017789.2:c.6676C>T (ATM) | XP_016873278.1:p.Leu2226= | |
| XM_017017790.2:c.6676C>T (ATM) | XP_016873279.1:p.Leu2226= | |
| NM_001330368.2:c.641-16342G>A (C11orf65) | NP_001317297.1:n.641-16342G>A | |
| NM_001351110.2:c.*38+9807G>A (C11orf65) | NP_001338039.1:n.*38+9807G>A | |
| NM_001351834.2:c.6676C>T (ATM) | NP_001338763.1:p.Leu2226= | |
| NM_000051.4:c.6676C>T (ATM) MANE Select | NP_000042.3:p.Leu2226= |