Canonical Allele Identifier: CA1998811954

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108334154_108334155delinsCT , CM000673.2:g.108334154_108334155delinsCT	GRCh38
NC_000011.9:g.108204881_108204882delinsCT , CM000673.1:g.108204881_108204882delinsCT	GRCh37
NC_000011.8:g.107710091_107710092delinsCT	NCBI36
NG_009830.1:g.116323_116324delinsCT , LRG_135:g.116323_116324delinsCT
NG_054724.1:g.140678_140679delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8010+186_8010+187delinsCT (ATM)	ENSP00000388058.2:n.8010+186_8010+187delinsCT
ENST00000713593.1:c.*7481+186_*7481+187delinsCT (ATM)	ENSP00000518889.1:n.*7481+186_*7481+187delinsCT
ENST00000278616.9:c.8010+186_8010+187delinsCT (ATM)	ENSP00000278616.4:n.8010+186_8010+187delinsCT
ENST00000525056.2:n.2429+186_2429+187delinsCT (ATM)
ENST00000638786.2:n.708+186_708+187delinsCT (ATM)
ENST00000682286.1:n.2767+186_2767+187delinsCT (ATM)
ENST00000682302.1:n.2428+186_2428+187delinsCT (ATM)
ENST00000683174.1:n.9494+186_9494+187delinsCT (ATM)
ENST00000683524.1:n.3234+186_3234+187delinsCT (ATM)
ENST00000684152.1:n.3426+186_3426+187delinsCT (ATM)
ENST00000684180.1:n.484+186_484+187delinsCT (ATM)
ENST00000684447.1:n.4503+186_4503+187delinsCT (ATM)
ENST00000527805.6:c.*3074+186_*3074+187delinsCT (ATM)	ENSP00000435747.2:n.*3074+186_*3074+187delinsCT
ENST00000675595.1:c.*3145+186_*3145+187delinsCT (ATM)	ENSP00000502563.1:n.*3145+186_*3145+187delinsCT
ENST00000675843.1:c.8010+186_8010+187delinsCT (ATM) MANE Select	ENSP00000501606.1:n.8010+186_8010+187delinsCT
ENST00000278616.8:c.8010+186_8010+187delinsCT (ATM)	ENSP00000278616.4:n.8010+186_8010+187delinsCT
ENST00000452508.6:c.8010+186_8010+187delinsCT (ATM)	ENSP00000388058.2:n.8010+186_8010+187delinsCT
ENST00000524755.5:c.299+1065_299+1066delinsAG (C11orf65)
ENST00000524792.5:n.4225+186_4225+187delinsCT (ATM)
ENST00000525056.1:n.207+186_207+187delinsCT (ATM)
ENST00000525729.5:c.641-25084_641-25083delinsAG (C11orf65)	ENSP00000433395.1:n.641-25084_641-25083delinsAG
ENST00000527531.5:c.*1269+1065_*1269+1066delinsAG (C11orf65)	ENSP00000431706.1:n.*1269+1065_*1269+1066delinsAG
ENST00000533979.5:n.222+186_222+187delinsCT (ATM)
ENST00000615746.4:c.*1269+1065_*1269+1066delinsAG (C11orf65)	ENSP00000483537.1:n.*1269+1065_*1269+1066delinsAG
NM_000051.3:c.8010+186_8010+187delinsCT , LRG_135t1:c.8010+186_8010+187delinsCT (ATM)	NP_000042.3:n.8010+186_8010+187delinsCT
XM_005271414.3:c.*38+1065_*38+1066delinsAG (C11orf65)	XP_005271471.1:n.*38+1065_*38+1066delinsAG
XM_005271415.3:c.804+1065_804+1066delinsAG (C11orf65)	XP_005271472.1:n.804+1065_804+1066delinsAG
XM_005271561.3:c.8010+186_8010+187delinsCT (ATM)	XP_005271618.2:n.8010+186_8010+187delinsCT
XM_005271562.3:c.8010+186_8010+187delinsCT (ATM)	XP_005271619.2:n.8010+186_8010+187delinsCT
XM_006718843.2:c.8010+186_8010+187delinsCT (ATM)	XP_006718906.1:n.8010+186_8010+187delinsCT
XM_006718845.1:c.3966+186_3966+187delinsCT (ATM)	XP_006718908.1:n.3966+186_3966+187delinsCT
XM_011542840.1:c.8010+186_8010+187delinsCT (ATM)	XP_011541142.1:n.8010+186_8010+187delinsCT
XM_011542841.1:c.8010+186_8010+187delinsCT (ATM)	XP_011541143.1:n.8010+186_8010+187delinsCT
XM_011542842.1:c.7845+186_7845+187delinsCT (ATM)	XP_011541144.1:n.7845+186_7845+187delinsCT
XM_011542843.1:c.8010+186_8010+187delinsCT (ATM)	XP_011541145.1:n.8010+186_8010+187delinsCT
XM_011542844.1:c.6966+186_6966+187delinsCT (ATM)	XP_011541146.1:n.6966+186_6966+187delinsCT
XM_011542845.1:c.6702+186_6702+187delinsCT (ATM)	XP_011541147.1:n.6702+186_6702+187delinsCT
XM_011542847.1:c.3081+186_3081+187delinsCT (ATM)	XP_011541149.1:n.3081+186_3081+187delinsCT
NM_001330368.1:c.641-25084_641-25083delinsAG (C11orf65)	NP_001317297.1:n.641-25084_641-25083delinsAG
NM_001351110.1:c.*38+1065_*38+1066delinsAG (C11orf65)	NP_001338039.1:n.*38+1065_*38+1066delinsAG
NM_001351834.1:c.8010+186_8010+187delinsCT (ATM)	NP_001338763.1:n.8010+186_8010+187delinsCT
NR_147053.2:n.2374+1065_2374+1066delinsAG (C11orf65)
XM_005271414.4:c.*38+1065_*38+1066delinsAG (C11orf65)	XP_005271471.1:n.*38+1065_*38+1066delinsAG
XM_005271415.4:c.804+1065_804+1066delinsAG (C11orf65)	XP_005271472.1:n.804+1065_804+1066delinsAG
XM_005271562.5:c.8010+186_8010+187delinsCT (ATM)	XP_005271619.2:n.8010+186_8010+187delinsCT
XM_006718843.4:c.8010+186_8010+187delinsCT (ATM)	XP_006718906.1:n.8010+186_8010+187delinsCT
XM_006718845.2:c.3966+186_3966+187delinsCT (ATM)	XP_006718908.1:n.3966+186_3966+187delinsCT
XM_011542840.3:c.8010+186_8010+187delinsCT (ATM)	XP_011541142.1:n.8010+186_8010+187delinsCT
XM_011542842.3:c.7845+186_7845+187delinsCT (ATM)	XP_011541144.1:n.7845+186_7845+187delinsCT
XM_011542843.2:c.8010+186_8010+187delinsCT (ATM)	XP_011541145.1:n.8010+186_8010+187delinsCT
XM_011542844.3:c.6966+186_6966+187delinsCT (ATM)	XP_011541146.1:n.6966+186_6966+187delinsCT
XM_011542845.2:c.6702+186_6702+187delinsCT (ATM)	XP_011541147.1:n.6702+186_6702+187delinsCT
XM_017017789.2:c.8010+186_8010+187delinsCT (ATM)	XP_016873278.1:n.8010+186_8010+187delinsCT
XM_017017790.2:c.8010+186_8010+187delinsCT (ATM)	XP_016873279.1:n.8010+186_8010+187delinsCT
NM_001330368.2:c.641-25084_641-25083delinsAG (C11orf65)	NP_001317297.1:n.641-25084_641-25083delinsAG
NM_001351110.2:c.*38+1065_*38+1066delinsAG (C11orf65)	NP_001338039.1:n.*38+1065_*38+1066delinsAG
NM_001351834.2:c.8010+186_8010+187delinsCT (ATM)	NP_001338763.1:n.8010+186_8010+187delinsCT
NM_000051.4:c.8010+186_8010+187delinsCT (ATM) MANE Select	NP_000042.3:n.8010+186_8010+187delinsCT
NR_147053.3:n.2372+1065_2372+1066delinsAG (C11orf65)