Canonical Allele Identifier: CA1998811376
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108332855_108332856delinsAT , CM000673.2:g.108332855_108332856delinsAT GRCh38
NC_000011.9:g.108203582_108203583delinsAT , CM000673.1:g.108203582_108203583delinsAT GRCh37
NC_000011.8:g.107708792_107708793delinsAT NCBI36
NG_009830.1:g.115024_115025delinsAT , LRG_135:g.115024_115025delinsAT
NG_054724.1:g.141977_141978delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.7882_7883delinsAT (ATM) ENSP00000388058.2:p.Ile2628=
ENST00000713593.1:c.*7353_*7354delinsAT (ATM) ENSP00000518889.1:n.*7353_*7354delinsAT
ENST00000278616.9:c.7882_7883delinsAT (ATM) ENSP00000278616.4:p.Ile2628=
ENST00000525056.2:n.2301_2302delinsAT (ATM)
ENST00000525537.3:n.1563_1564delinsAT (ATM)
ENST00000638786.2:n.625+818_625+819delinsAT (ATM)
ENST00000682286.1:n.2639_2640delinsAT (ATM)
ENST00000682302.1:n.2300_2301delinsAT (ATM)
ENST00000683174.1:n.9366_9367delinsAT (ATM)
ENST00000683524.1:n.3106_3107delinsAT (ATM)
ENST00000684152.1:n.3344-1031_3344-1030delinsAT (ATM)
ENST00000684180.1:n.356_357delinsAT (ATM)
ENST00000684447.1:n.3390_3391delinsAT (ATM)
ENST00000527805.6:c.*2946_*2947delinsAT (ATM) ENSP00000435747.2:n.*2946_*2947delinsAT
ENST00000675595.1:c.*3017_*3018delinsAT (ATM) ENSP00000502563.1:n.*3017_*3018delinsAT
ENST00000675843.1:c.7882_7883delinsAT (ATM) MANE Select ENSP00000501606.1:p.Ile2628=
ENST00000278616.8:c.7882_7883delinsAT (ATM) ENSP00000278616.4:p.Ile2628=
ENST00000452508.6:c.7882_7883delinsAT (ATM) ENSP00000388058.2:p.Ile2628=
ENST00000524755.5:c.300-1289_300-1288delinsAT (C11orf65)
ENST00000524792.5:n.4097_4098delinsAT (ATM)
ENST00000525056.1:n.79_80delinsAT (ATM)
ENST00000525729.5:c.641-23785_641-23784delinsAT (C11orf65) ENSP00000433395.1:n.641-23785_641-23784delinsAT
ENST00000527531.5:c.*1270-1289_*1270-1288delinsAT (C11orf65) ENSP00000431706.1:n.*1270-1289_*1270-1288delinsAT
ENST00000533690.5:n.3286_3287delinsAT (ATM)
ENST00000533979.5:n.94_95delinsAT (ATM)
ENST00000615746.4:c.*1270-1289_*1270-1288delinsAT (C11orf65) ENSP00000483537.1:n.*1270-1289_*1270-1288delinsAT
NM_000051.3:c.7882_7883delinsAT , LRG_135t1:c.7882_7883delinsAT (ATM) NP_000042.3:p.Ile2628=
XM_005271414.3:c.*39-1289_*39-1288delinsAT (C11orf65) XP_005271471.1:n.*39-1289_*39-1288delinsAT
XM_005271415.3:c.805-1289_805-1288delinsAT (C11orf65) XP_005271472.1:n.805-1289_805-1288delinsAT
XM_005271561.3:c.7882_7883delinsAT (ATM) XP_005271618.2:p.Ile2628=
XM_005271562.3:c.7882_7883delinsAT (ATM) XP_005271619.2:p.Ile2628=
XM_006718843.2:c.7882_7883delinsAT (ATM) XP_006718906.1:p.Ile2628=
XM_006718845.1:c.3838_3839delinsAT (ATM) XP_006718908.1:p.Ile1280=
XM_011542840.1:c.7882_7883delinsAT (ATM) XP_011541142.1:p.Ile2628=
XM_011542841.1:c.7882_7883delinsAT (ATM) XP_011541143.1:p.Ile2628=
XM_011542842.1:c.7717_7718delinsAT (ATM) XP_011541144.1:p.Ile2573=
XM_011542843.1:c.7882_7883delinsAT (ATM) XP_011541145.1:p.Ile2628=
XM_011542844.1:c.6838_6839delinsAT (ATM) XP_011541146.1:p.Ile2280=
XM_011542845.1:c.6574_6575delinsAT (ATM) XP_011541147.1:p.Ile2192=
XM_011542847.1:c.2953_2954delinsAT (ATM) XP_011541149.1:p.Ile985=
NM_001330368.1:c.641-23785_641-23784delinsAT (C11orf65) NP_001317297.1:n.641-23785_641-23784delinsAT
NM_001351110.1:c.*38+2364_*38+2365delinsAT (C11orf65) NP_001338039.1:n.*38+2364_*38+2365delinsAT
NM_001351834.1:c.7882_7883delinsAT (ATM) NP_001338763.1:p.Ile2628=
NR_147053.2:n.2375-1289_2375-1288delinsAT (C11orf65)
XM_005271414.4:c.*39-1289_*39-1288delinsAT (C11orf65) XP_005271471.1:n.*39-1289_*39-1288delinsAT
XM_005271415.4:c.805-1289_805-1288delinsAT (C11orf65) XP_005271472.1:n.805-1289_805-1288delinsAT
XM_005271562.5:c.7882_7883delinsAT (ATM) XP_005271619.2:p.Ile2628=
XM_006718843.4:c.7882_7883delinsAT (ATM) XP_006718906.1:p.Ile2628=
XM_006718845.2:c.3838_3839delinsAT (ATM) XP_006718908.1:p.Ile1280=
XM_011542840.3:c.7882_7883delinsAT (ATM) XP_011541142.1:p.Ile2628=
XM_011542842.3:c.7717_7718delinsAT (ATM) XP_011541144.1:p.Ile2573=
XM_011542843.2:c.7882_7883delinsAT (ATM) XP_011541145.1:p.Ile2628=
XM_011542844.3:c.6838_6839delinsAT (ATM) XP_011541146.1:p.Ile2280=
XM_011542845.2:c.6574_6575delinsAT (ATM) XP_011541147.1:p.Ile2192=
XM_017017789.2:c.7882_7883delinsAT (ATM) XP_016873278.1:p.Ile2628=
XM_017017790.2:c.7882_7883delinsAT (ATM) XP_016873279.1:p.Ile2628=
NM_001330368.2:c.641-23785_641-23784delinsAT (C11orf65) NP_001317297.1:n.641-23785_641-23784delinsAT
NM_001351110.2:c.*38+2364_*38+2365delinsAT (C11orf65) NP_001338039.1:n.*38+2364_*38+2365delinsAT
NM_001351834.2:c.7882_7883delinsAT (ATM) NP_001338763.1:p.Ile2628=
NM_000051.4:c.7882_7883delinsAT (ATM) MANE Select NP_000042.3:p.Ile2628=
NR_147053.3:n.2373-1289_2373-1288delinsAT (C11orf65)