Canonical Allele Identifier: CA2574971095
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108317274_108317275del , CM000673.2:g.108317274_108317275del GRCh38
NC_000011.9:g.108188001_108188002del , CM000673.1:g.108188001_108188002del GRCh37
NC_000011.8:g.107693211_107693212del NCBI36
NG_009830.1:g.99443_99444del , LRG_135:g.99443_99444del
NG_054724.1:g.157560_157561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.6199-99_6199-98del (ATM) ENSP00000388058.2:n.6199-99_6199-98del
ENST00000713593.1:c.*5670-99_*5670-98del (ATM) ENSP00000518889.1:n.*5670-99_*5670-98del
ENST00000278616.9:c.6199-99_6199-98del (ATM) ENSP00000278616.4:n.6199-99_6199-98del
ENST00000525056.2:n.618-99_618-98del (ATM)
ENST00000682286.1:n.956-99_956-98del (ATM)
ENST00000682302.1:n.617-99_617-98del (ATM)
ENST00000683174.1:n.7683-99_7683-98del (ATM)
ENST00000683524.1:n.1423-99_1423-98del (ATM)
ENST00000684152.1:n.1913-99_1913-98del (ATM)
ENST00000527805.6:c.*1263-99_*1263-98del (ATM) ENSP00000435747.2:n.*1263-99_*1263-98del
ENST00000675595.1:c.*1263-99_*1263-98del (ATM) ENSP00000502563.1:n.*1263-99_*1263-98del
ENST00000675843.1:c.6199-99_6199-98del (ATM) MANE Select ENSP00000501606.1:n.6199-99_6199-98del
ENST00000278616.8:c.6199-99_6199-98del (ATM) ENSP00000278616.4:n.6199-99_6199-98del
ENST00000452508.6:c.6199-99_6199-98del (ATM) ENSP00000388058.2:n.6199-99_6199-98del
ENST00000524792.5:n.2414-99_2414-98del (ATM)
ENST00000525729.5:c.641-8202_641-8201del (C11orf65) ENSP00000433395.1:n.641-8202_641-8201del
ENST00000532765.1:n.516-99_516-98del (ATM)
ENST00000533690.5:n.1603-99_1603-98del (ATM)
NM_000051.3:c.6199-99_6199-98del , LRG_135t1:c.6199-99_6199-98del (ATM) NP_000042.3:n.6199-99_6199-98del
XM_005271561.3:c.6199-99_6199-98del (ATM) XP_005271618.2:n.6199-99_6199-98del
XM_005271562.3:c.6199-99_6199-98del (ATM) XP_005271619.2:n.6199-99_6199-98del
XM_006718843.2:c.6199-99_6199-98del (ATM) XP_006718906.1:n.6199-99_6199-98del
XM_006718845.1:c.2155-99_2155-98del (ATM) XP_006718908.1:n.2155-99_2155-98del
XM_011542840.1:c.6199-99_6199-98del (ATM) XP_011541142.1:n.6199-99_6199-98del
XM_011542841.1:c.6199-99_6199-98del (ATM) XP_011541143.1:n.6199-99_6199-98del
XM_011542842.1:c.6034-99_6034-98del (ATM) XP_011541144.1:n.6034-99_6034-98del
XM_011542843.1:c.6199-99_6199-98del (ATM) XP_011541145.1:n.6199-99_6199-98del
XM_011542844.1:c.5155-99_5155-98del (ATM) XP_011541146.1:n.5155-99_5155-98del
XM_011542845.1:c.4891-99_4891-98del (ATM) XP_011541147.1:n.4891-99_4891-98del
XM_011542847.1:c.1270-99_1270-98del (ATM) XP_011541149.1:n.1270-99_1270-98del
NM_001330368.1:c.641-8202_641-8201del (C11orf65) NP_001317297.1:n.641-8202_641-8201del
NM_001351110.1:c.*39-8202_*39-8201del (C11orf65) NP_001338039.1:n.*39-8202_*39-8201del
NM_001351834.1:c.6199-99_6199-98del (ATM) NP_001338763.1:n.6199-99_6199-98del
XM_005271562.5:c.6199-99_6199-98del (ATM) XP_005271619.2:n.6199-99_6199-98del
XM_006718843.4:c.6199-99_6199-98del (ATM) XP_006718906.1:n.6199-99_6199-98del
XM_006718845.2:c.2155-99_2155-98del (ATM) XP_006718908.1:n.2155-99_2155-98del
XM_011542840.3:c.6199-99_6199-98del (ATM) XP_011541142.1:n.6199-99_6199-98del
XM_011542842.3:c.6034-99_6034-98del (ATM) XP_011541144.1:n.6034-99_6034-98del
XM_011542843.2:c.6199-99_6199-98del (ATM) XP_011541145.1:n.6199-99_6199-98del
XM_011542844.3:c.5155-99_5155-98del (ATM) XP_011541146.1:n.5155-99_5155-98del
XM_011542845.2:c.4891-99_4891-98del (ATM) XP_011541147.1:n.4891-99_4891-98del
XM_017017789.2:c.6199-99_6199-98del (ATM) XP_016873278.1:n.6199-99_6199-98del
XM_017017790.2:c.6199-99_6199-98del (ATM) XP_016873279.1:n.6199-99_6199-98del
XM_017017791.1:c.6199-99_6199-98del (ATM) XP_016873280.1:n.6199-99_6199-98del
NM_001330368.2:c.641-8202_641-8201del (C11orf65) NP_001317297.1:n.641-8202_641-8201del
NM_001351110.2:c.*39-8202_*39-8201del (C11orf65) NP_001338039.1:n.*39-8202_*39-8201del
NM_001351834.2:c.6199-99_6199-98del (ATM) NP_001338763.1:n.6199-99_6199-98del
NM_000051.4:c.6199-99_6199-98del (ATM) MANE Select NP_000042.3:n.6199-99_6199-98del