Canonical Allele Identifier: CA1998805573
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108320093_108320094delinsAT , CM000673.2:g.108320093_108320094delinsAT GRCh38
NC_000011.9:g.108190820_108190821delinsAT , CM000673.1:g.108190820_108190821delinsAT GRCh37
NC_000011.8:g.107696030_107696031delinsAT NCBI36
NG_009830.1:g.102262_102263delinsAT , LRG_135:g.102262_102263delinsAT
NG_054724.1:g.154739_154740delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.6452+35_6452+36delinsAT (ATM) ENSP00000388058.2:n.6452+35_6452+36delinsAT
ENST00000713593.1:c.*5923+35_*5923+36delinsAT (ATM) ENSP00000518889.1:n.*5923+35_*5923+36delinsAT
ENST00000278616.9:c.6452+35_6452+36delinsAT (ATM) ENSP00000278616.4:n.6452+35_6452+36delinsAT
ENST00000525056.2:n.871+35_871+36delinsAT (ATM)
ENST00000682286.1:n.1209+35_1209+36delinsAT (ATM)
ENST00000682302.1:n.870+35_870+36delinsAT (ATM)
ENST00000683174.1:n.7936+35_7936+36delinsAT (ATM)
ENST00000683524.1:n.1676+35_1676+36delinsAT (ATM)
ENST00000684152.1:n.2166+35_2166+36delinsAT (ATM)
ENST00000527805.6:c.*1516+35_*1516+36delinsAT (ATM) ENSP00000435747.2:n.*1516+35_*1516+36delinsAT
ENST00000675595.1:c.*1516+35_*1516+36delinsAT (ATM) ENSP00000502563.1:n.*1516+35_*1516+36delinsAT
ENST00000675843.1:c.6452+35_6452+36delinsAT (ATM) MANE Select ENSP00000501606.1:n.6452+35_6452+36delinsAT
ENST00000278616.8:c.6452+35_6452+36delinsAT (ATM) ENSP00000278616.4:n.6452+35_6452+36delinsAT
ENST00000452508.6:c.6452+35_6452+36delinsAT (ATM) ENSP00000388058.2:n.6452+35_6452+36delinsAT
ENST00000524792.5:n.2667+35_2667+36delinsAT (ATM)
ENST00000525729.5:c.641-11023_641-11022delinsAT (C11orf65) ENSP00000433395.1:n.641-11023_641-11022delinsAT
ENST00000533690.5:n.1856+35_1856+36delinsAT (ATM)
NM_000051.3:c.6452+35_6452+36delinsAT , LRG_135t1:c.6452+35_6452+36delinsAT (ATM) NP_000042.3:n.6452+35_6452+36delinsAT
XM_005271561.3:c.6452+35_6452+36delinsAT (ATM) XP_005271618.2:n.6452+35_6452+36delinsAT
XM_005271562.3:c.6452+35_6452+36delinsAT (ATM) XP_005271619.2:n.6452+35_6452+36delinsAT
XM_006718843.2:c.6452+35_6452+36delinsAT (ATM) XP_006718906.1:n.6452+35_6452+36delinsAT
XM_006718845.1:c.2408+35_2408+36delinsAT (ATM) XP_006718908.1:n.2408+35_2408+36delinsAT
XM_011542840.1:c.6452+35_6452+36delinsAT (ATM) XP_011541142.1:n.6452+35_6452+36delinsAT
XM_011542841.1:c.6452+35_6452+36delinsAT (ATM) XP_011541143.1:n.6452+35_6452+36delinsAT
XM_011542842.1:c.6287+35_6287+36delinsAT (ATM) XP_011541144.1:n.6287+35_6287+36delinsAT
XM_011542843.1:c.6452+35_6452+36delinsAT (ATM) XP_011541145.1:n.6452+35_6452+36delinsAT
XM_011542844.1:c.5408+35_5408+36delinsAT (ATM) XP_011541146.1:n.5408+35_5408+36delinsAT
XM_011542845.1:c.5144+35_5144+36delinsAT (ATM) XP_011541147.1:n.5144+35_5144+36delinsAT
XM_011542847.1:c.1523+35_1523+36delinsAT (ATM) XP_011541149.1:n.1523+35_1523+36delinsAT
NM_001330368.1:c.641-11023_641-11022delinsAT (C11orf65) NP_001317297.1:n.641-11023_641-11022delinsAT
NM_001351110.1:c.*39-11023_*39-11022delinsAT (C11orf65) NP_001338039.1:n.*39-11023_*39-11022delinsAT
NM_001351834.1:c.6452+35_6452+36delinsAT (ATM) NP_001338763.1:n.6452+35_6452+36delinsAT
XM_005271562.5:c.6452+35_6452+36delinsAT (ATM) XP_005271619.2:n.6452+35_6452+36delinsAT
XM_006718843.4:c.6452+35_6452+36delinsAT (ATM) XP_006718906.1:n.6452+35_6452+36delinsAT
XM_006718845.2:c.2408+35_2408+36delinsAT (ATM) XP_006718908.1:n.2408+35_2408+36delinsAT
XM_011542840.3:c.6452+35_6452+36delinsAT (ATM) XP_011541142.1:n.6452+35_6452+36delinsAT
XM_011542842.3:c.6287+35_6287+36delinsAT (ATM) XP_011541144.1:n.6287+35_6287+36delinsAT
XM_011542843.2:c.6452+35_6452+36delinsAT (ATM) XP_011541145.1:n.6452+35_6452+36delinsAT
XM_011542844.3:c.5408+35_5408+36delinsAT (ATM) XP_011541146.1:n.5408+35_5408+36delinsAT
XM_011542845.2:c.5144+35_5144+36delinsAT (ATM) XP_011541147.1:n.5144+35_5144+36delinsAT
XM_017017789.2:c.6452+35_6452+36delinsAT (ATM) XP_016873278.1:n.6452+35_6452+36delinsAT
XM_017017790.2:c.6452+35_6452+36delinsAT (ATM) XP_016873279.1:n.6452+35_6452+36delinsAT
XM_017017791.1:c.6452+35_6452+36delinsAT (ATM) XP_016873280.1:n.6452+35_6452+36delinsAT
NM_001330368.2:c.641-11023_641-11022delinsAT (C11orf65) NP_001317297.1:n.641-11023_641-11022delinsAT
NM_001351110.2:c.*39-11023_*39-11022delinsAT (C11orf65) NP_001338039.1:n.*39-11023_*39-11022delinsAT
NM_001351834.2:c.6452+35_6452+36delinsAT (ATM) NP_001338763.1:n.6452+35_6452+36delinsAT
NM_000051.4:c.6452+35_6452+36delinsAT (ATM) MANE Select NP_000042.3:n.6452+35_6452+36delinsAT