MyVariant.info:
GRCh37
chr11:g.108206574C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108335847C>A , CM000673.2:g.108335847C>A | GRCh38 |
| NC_000011.9:g.108206574C>A , CM000673.1:g.108206574C>A | GRCh37 |
| NC_000011.8:g.107711784C>A | NCBI36 |
| NG_009830.1:g.118016C>A , LRG_135:g.118016C>A | |
| NG_054724.1:g.138986G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8154C>A (ATM) | ENSP00000388058.2:p.Gly2718= | |
| ENST00000713593.1:c.*7625C>A (ATM) | ENSP00000518889.1:n.*7625C>A | |
| ENST00000278616.9:c.8154C>A (ATM) | ENSP00000278616.4:p.Gly2718= | |
| ENST00000525056.2:n.2573C>A (ATM) | ||
| ENST00000638786.2:n.852C>A (ATM) | ||
| ENST00000682286.1:n.2911C>A (ATM) | ||
| ENST00000682302.1:n.2572C>A (ATM) | ||
| ENST00000683174.1:n.9638C>A (ATM) | ||
| ENST00000683524.1:n.3378C>A (ATM) | ||
| ENST00000684152.1:n.3570C>A (ATM) | ||
| ENST00000684180.1:n.628C>A (ATM) | ||
| ENST00000684447.1:n.4647C>A (ATM) | ||
| ENST00000527805.6:c.*3218C>A (ATM) | ENSP00000435747.2:n.*3218C>A | |
| ENST00000675595.1:c.*3289C>A (ATM) | ENSP00000502563.1:n.*3289C>A | |
| ENST00000675843.1:c.8154C>A (ATM) MANE Select | ENSP00000501606.1:p.Gly2718= | |
| ENST00000278616.8:c.8154C>A (ATM) | ENSP00000278616.4:p.Gly2718= | |
| ENST00000452508.6:c.8154C>A (ATM) | ENSP00000388058.2:p.Gly2718= | |
| ENST00000524755.5:c.227-555G>T (C11orf65) | ||
| ENST00000524792.5:n.4369C>A (ATM) | ||
| ENST00000525056.1:n.351C>A (ATM) | ||
| ENST00000525729.5:c.641-26776G>T (C11orf65) | ENSP00000433395.1:n.641-26776G>T | |
| ENST00000527531.5:c.*1197-555G>T (C11orf65) | ENSP00000431706.1:n.*1197-555G>T | |
| ENST00000533979.5:n.366C>A (ATM) | ||
| ENST00000615746.4:c.*1197-555G>T (C11orf65) | ENSP00000483537.1:n.*1197-555G>T | |
| NM_000051.3:c.8154C>A , LRG_135t1:c.8154C>A (ATM) | NP_000042.3:p.Gly2718= | |
| XM_005271414.3:c.788-555G>T (C11orf65) | XP_005271471.1:n.788-555G>T | |
| XM_005271415.3:c.732-555G>T (C11orf65) | XP_005271472.1:n.732-555G>T | |
| XM_005271561.3:c.8154C>A (ATM) | XP_005271618.2:p.Gly2718= | |
| XM_005271562.3:c.8154C>A (ATM) | XP_005271619.2:p.Gly2718= | |
| XM_006718843.2:c.8154C>A (ATM) | XP_006718906.1:p.Gly2718= | |
| XM_006718845.1:c.4110C>A (ATM) | XP_006718908.1:p.Gly1370= | |
| XM_011542840.1:c.8154C>A (ATM) | XP_011541142.1:p.Gly2718= | |
| XM_011542841.1:c.8154C>A (ATM) | XP_011541143.1:p.Gly2718= | |
| XM_011542842.1:c.7989C>A (ATM) | XP_011541144.1:p.Gly2663= | |
| XM_011542843.1:c.8154C>A (ATM) | XP_011541145.1:p.Gly2718= | |
| XM_011542844.1:c.7110C>A (ATM) | XP_011541146.1:p.Gly2370= | |
| XM_011542845.1:c.6846C>A (ATM) | XP_011541147.1:p.Gly2282= | |
| XM_011542847.1:c.3225C>A (ATM) | XP_011541149.1:p.Gly1075= | |
| NM_001330368.1:c.641-26776G>T (C11orf65) | NP_001317297.1:n.641-26776G>T | |
| NM_001351110.1:c.695-555G>T (C11orf65) | NP_001338039.1:n.695-555G>T | |
| NM_001351834.1:c.8154C>A (ATM) | NP_001338763.1:p.Gly2718= | |
| NR_147053.2:n.2302-555G>T (C11orf65) | ||
| XM_005271414.4:c.788-555G>T (C11orf65) | XP_005271471.1:n.788-555G>T | |
| XM_005271415.4:c.732-555G>T (C11orf65) | XP_005271472.1:n.732-555G>T | |
| XM_005271562.5:c.8154C>A (ATM) | XP_005271619.2:p.Gly2718= | |
| XM_006718843.4:c.8154C>A (ATM) | XP_006718906.1:p.Gly2718= | |
| XM_006718845.2:c.4110C>A (ATM) | XP_006718908.1:p.Gly1370= | |
| XM_011542840.3:c.8154C>A (ATM) | XP_011541142.1:p.Gly2718= | |
| XM_011542842.3:c.7989C>A (ATM) | XP_011541144.1:p.Gly2663= | |
| XM_011542843.2:c.8154C>A (ATM) | XP_011541145.1:p.Gly2718= | |
| XM_011542844.3:c.7110C>A (ATM) | XP_011541146.1:p.Gly2370= | |
| XM_011542845.2:c.6846C>A (ATM) | XP_011541147.1:p.Gly2282= | |
| XM_017017789.2:c.8154C>A (ATM) | XP_016873278.1:p.Gly2718= | |
| XM_017017790.2:c.8154C>A (ATM) | XP_016873279.1:p.Gly2718= | |
| NM_001330368.2:c.641-26776G>T (C11orf65) | NP_001317297.1:n.641-26776G>T | |
| NM_001351110.2:c.695-555G>T (C11orf65) | NP_001338039.1:n.695-555G>T | |
| NM_001351834.2:c.8154C>A (ATM) | NP_001338763.1:p.Gly2718= | |
| NM_000051.4:c.8154C>A (ATM) MANE Select | NP_000042.3:p.Gly2718= | |
| NR_147053.3:n.2300-555G>T (C11orf65) |