Canonical Allele Identifier: CA1998812341
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108335036_108335039delinsCAGG , CM000673.2:g.108335036_108335039delinsCAGG GRCh38
NC_000011.9:g.108205763_108205766delinsCAGG , CM000673.1:g.108205763_108205766delinsCAGG GRCh37
NC_000011.8:g.107710973_107710976delinsCAGG NCBI36
NG_009830.1:g.117205_117208delinsCAGG , LRG_135:g.117205_117208delinsCAGG
NG_054724.1:g.139794_139797delinsCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.8078_8081delinsCAGG (ATM) ENSP00000388058.2:p.Ala2693=
ENST00000713593.1:c.*7549_*7552delinsCAGG (ATM) ENSP00000518889.1:n.*7549_*7552delinsCAGG
ENST00000278616.9:c.8078_8081delinsCAGG (ATM) ENSP00000278616.4:p.Ala2693=
ENST00000525056.2:n.2497_2500delinsCAGG (ATM)
ENST00000638786.2:n.776_779delinsCAGG (ATM)
ENST00000682286.1:n.2835_2838delinsCAGG (ATM)
ENST00000682302.1:n.2496_2499delinsCAGG (ATM)
ENST00000683174.1:n.9562_9565delinsCAGG (ATM)
ENST00000683524.1:n.3302_3305delinsCAGG (ATM)
ENST00000684152.1:n.3494_3497delinsCAGG (ATM)
ENST00000684180.1:n.552_555delinsCAGG (ATM)
ENST00000684447.1:n.4571_4574delinsCAGG (ATM)
ENST00000527805.6:c.*3142_*3145delinsCAGG (ATM) ENSP00000435747.2:n.*3142_*3145delinsCAGG
ENST00000675595.1:c.*3213_*3216delinsCAGG (ATM) ENSP00000502563.1:n.*3213_*3216delinsCAGG
ENST00000675843.1:c.8078_8081delinsCAGG (ATM) MANE Select ENSP00000501606.1:p.Ala2693=
ENST00000278616.8:c.8078_8081delinsCAGG (ATM) ENSP00000278616.4:p.Ala2693=
ENST00000452508.6:c.8078_8081delinsCAGG (ATM) ENSP00000388058.2:p.Ala2693=
ENST00000524755.5:c.299+181_299+184delinsCCTG (C11orf65)
ENST00000524792.5:n.4293_4296delinsCAGG (ATM)
ENST00000525056.1:n.275_278delinsCAGG (ATM)
ENST00000525729.5:c.641-25968_641-25965delinsCCTG (C11orf65) ENSP00000433395.1:n.641-25968_641-25965delinsCCTG
ENST00000527531.5:c.*1269+181_*1269+184delinsCCTG (C11orf65) ENSP00000431706.1:n.*1269+181_*1269+184delinsCCTG
ENST00000533979.5:n.290_293delinsCAGG (ATM)
ENST00000615746.4:c.*1269+181_*1269+184delinsCCTG (C11orf65) ENSP00000483537.1:n.*1269+181_*1269+184delinsCCTG
NM_000051.3:c.8078_8081delinsCAGG , LRG_135t1:c.8078_8081delinsCAGG (ATM) NP_000042.3:p.Ala2693=
XM_005271414.3:c.*38+181_*38+184delinsCCTG (C11orf65) XP_005271471.1:n.*38+181_*38+184delinsCCTG
XM_005271415.3:c.804+181_804+184delinsCCTG (C11orf65) XP_005271472.1:n.804+181_804+184delinsCCTG
XM_005271561.3:c.8078_8081delinsCAGG (ATM) XP_005271618.2:p.Ala2693=
XM_005271562.3:c.8078_8081delinsCAGG (ATM) XP_005271619.2:p.Ala2693=
XM_006718843.2:c.8078_8081delinsCAGG (ATM) XP_006718906.1:p.Ala2693=
XM_006718845.1:c.4034_4037delinsCAGG (ATM) XP_006718908.1:p.Ala1345=
XM_011542840.1:c.8078_8081delinsCAGG (ATM) XP_011541142.1:p.Ala2693=
XM_011542841.1:c.8078_8081delinsCAGG (ATM) XP_011541143.1:p.Ala2693=
XM_011542842.1:c.7913_7916delinsCAGG (ATM) XP_011541144.1:p.Ala2638=
XM_011542843.1:c.8078_8081delinsCAGG (ATM) XP_011541145.1:p.Ala2693=
XM_011542844.1:c.7034_7037delinsCAGG (ATM) XP_011541146.1:p.Ala2345=
XM_011542845.1:c.6770_6773delinsCAGG (ATM) XP_011541147.1:p.Ala2257=
XM_011542847.1:c.3149_3152delinsCAGG (ATM) XP_011541149.1:p.Ala1050=
NM_001330368.1:c.641-25968_641-25965delinsCCTG (C11orf65) NP_001317297.1:n.641-25968_641-25965delinsCCTG
NM_001351110.1:c.*38+181_*38+184delinsCCTG (C11orf65) NP_001338039.1:n.*38+181_*38+184delinsCCTG
NM_001351834.1:c.8078_8081delinsCAGG (ATM) NP_001338763.1:p.Ala2693=
NR_147053.2:n.2374+181_2374+184delinsCCTG (C11orf65)
XM_005271414.4:c.*38+181_*38+184delinsCCTG (C11orf65) XP_005271471.1:n.*38+181_*38+184delinsCCTG
XM_005271415.4:c.804+181_804+184delinsCCTG (C11orf65) XP_005271472.1:n.804+181_804+184delinsCCTG
XM_005271562.5:c.8078_8081delinsCAGG (ATM) XP_005271619.2:p.Ala2693=
XM_006718843.4:c.8078_8081delinsCAGG (ATM) XP_006718906.1:p.Ala2693=
XM_006718845.2:c.4034_4037delinsCAGG (ATM) XP_006718908.1:p.Ala1345=
XM_011542840.3:c.8078_8081delinsCAGG (ATM) XP_011541142.1:p.Ala2693=
XM_011542842.3:c.7913_7916delinsCAGG (ATM) XP_011541144.1:p.Ala2638=
XM_011542843.2:c.8078_8081delinsCAGG (ATM) XP_011541145.1:p.Ala2693=
XM_011542844.3:c.7034_7037delinsCAGG (ATM) XP_011541146.1:p.Ala2345=
XM_011542845.2:c.6770_6773delinsCAGG (ATM) XP_011541147.1:p.Ala2257=
XM_017017789.2:c.8078_8081delinsCAGG (ATM) XP_016873278.1:p.Ala2693=
XM_017017790.2:c.8078_8081delinsCAGG (ATM) XP_016873279.1:p.Ala2693=
NM_001330368.2:c.641-25968_641-25965delinsCCTG (C11orf65) NP_001317297.1:n.641-25968_641-25965delinsCCTG
NM_001351110.2:c.*38+181_*38+184delinsCCTG (C11orf65) NP_001338039.1:n.*38+181_*38+184delinsCCTG
NM_001351834.2:c.8078_8081delinsCAGG (ATM) NP_001338763.1:p.Ala2693=
NM_000051.4:c.8078_8081delinsCAGG (ATM) MANE Select NP_000042.3:p.Ala2693=
NR_147053.3:n.2372+181_2372+184delinsCCTG (C11orf65)