Canonical Allele Identifier: CA1998805534
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108320017_108320019delinsCAG , CM000673.2:g.108320017_108320019delinsCAG GRCh38
NC_000011.9:g.108190744_108190746delinsCAG , CM000673.1:g.108190744_108190746delinsCAG GRCh37
NC_000011.8:g.107695954_107695956delinsCAG NCBI36
NG_009830.1:g.102186_102188delinsCAG , LRG_135:g.102186_102188delinsCAG
NG_054724.1:g.154814_154816delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.6411_6413delinsCAG (ATM) ENSP00000388058.2:p.Asp2137=
ENST00000713593.1:c.*5882_*5884delinsCAG (ATM) ENSP00000518889.1:n.*5882_*5884delinsCAG
ENST00000278616.9:c.6411_6413delinsCAG (ATM) ENSP00000278616.4:p.Asp2137=
ENST00000525056.2:n.830_832delinsCAG (ATM)
ENST00000682286.1:n.1168_1170delinsCAG (ATM)
ENST00000682302.1:n.829_831delinsCAG (ATM)
ENST00000683174.1:n.7895_7897delinsCAG (ATM)
ENST00000683524.1:n.1635_1637delinsCAG (ATM)
ENST00000684152.1:n.2125_2127delinsCAG (ATM)
ENST00000527805.6:c.*1475_*1477delinsCAG (ATM) ENSP00000435747.2:n.*1475_*1477delinsCAG
ENST00000675595.1:c.*1475_*1477delinsCAG (ATM) ENSP00000502563.1:n.*1475_*1477delinsCAG
ENST00000675843.1:c.6411_6413delinsCAG (ATM) MANE Select ENSP00000501606.1:p.Asp2137=
ENST00000278616.8:c.6411_6413delinsCAG (ATM) ENSP00000278616.4:p.Asp2137=
ENST00000452508.6:c.6411_6413delinsCAG (ATM) ENSP00000388058.2:p.Asp2137=
ENST00000524792.5:n.2626_2628delinsCAG (ATM)
ENST00000525729.5:c.641-10948_641-10946delinsCTG (C11orf65) ENSP00000433395.1:n.641-10948_641-10946de...
ENST00000533690.5:n.1815_1817delinsCAG (ATM)
NM_000051.3:c.6411_6413delinsCAG , LRG_135t1:c.6411_6413delinsCAG (ATM) NP_000042.3:p.Asp2137=
XM_005271561.3:c.6411_6413delinsCAG (ATM) XP_005271618.2:p.Asp2137=
XM_005271562.3:c.6411_6413delinsCAG (ATM) XP_005271619.2:p.Asp2137=
XM_006718843.2:c.6411_6413delinsCAG (ATM) XP_006718906.1:p.Asp2137=
XM_006718845.1:c.2367_2369delinsCAG (ATM) XP_006718908.1:p.Asp789=
XM_011542840.1:c.6411_6413delinsCAG (ATM) XP_011541142.1:p.Asp2137=
XM_011542841.1:c.6411_6413delinsCAG (ATM) XP_011541143.1:p.Asp2137=
XM_011542842.1:c.6246_6248delinsCAG (ATM) XP_011541144.1:p.Asp2082=
XM_011542843.1:c.6411_6413delinsCAG (ATM) XP_011541145.1:p.Asp2137=
XM_011542844.1:c.5367_5369delinsCAG (ATM) XP_011541146.1:p.Asp1789=
XM_011542845.1:c.5103_5105delinsCAG (ATM) XP_011541147.1:p.Asp1701=
XM_011542847.1:c.1482_1484delinsCAG (ATM) XP_011541149.1:p.Asp494=
NM_001330368.1:c.641-10948_641-10946delinsCTG (C11orf65) NP_001317297.1:n.641-10948_641-10946delin...
NM_001351110.1:c.*39-10948_*39-10946delinsCTG (C11orf65) NP_001338039.1:n.*39-10948_*39-10946delin...
NM_001351834.1:c.6411_6413delinsCAG (ATM) NP_001338763.1:p.Asp2137=
XM_005271562.5:c.6411_6413delinsCAG (ATM) XP_005271619.2:p.Asp2137=
XM_006718843.4:c.6411_6413delinsCAG (ATM) XP_006718906.1:p.Asp2137=
XM_006718845.2:c.2367_2369delinsCAG (ATM) XP_006718908.1:p.Asp789=
XM_011542840.3:c.6411_6413delinsCAG (ATM) XP_011541142.1:p.Asp2137=
XM_011542842.3:c.6246_6248delinsCAG (ATM) XP_011541144.1:p.Asp2082=
XM_011542843.2:c.6411_6413delinsCAG (ATM) XP_011541145.1:p.Asp2137=
XM_011542844.3:c.5367_5369delinsCAG (ATM) XP_011541146.1:p.Asp1789=
XM_011542845.2:c.5103_5105delinsCAG (ATM) XP_011541147.1:p.Asp1701=
XM_017017789.2:c.6411_6413delinsCAG (ATM) XP_016873278.1:p.Asp2137=
XM_017017790.2:c.6411_6413delinsCAG (ATM) XP_016873279.1:p.Asp2137=
XM_017017791.1:c.6411_6413delinsCAG (ATM) XP_016873280.1:p.Asp2137=
NM_001330368.2:c.641-10948_641-10946delinsCTG (C11orf65) NP_001317297.1:n.641-10948_641-10946delin...
NM_001351110.2:c.*39-10948_*39-10946delinsCTG (C11orf65) NP_001338039.1:n.*39-10948_*39-10946delin...
NM_001351834.2:c.6411_6413delinsCAG (ATM) NP_001338763.1:p.Asp2137=
NM_000051.4:c.6411_6413delinsCAG (ATM) MANE Select NP_000042.3:p.Asp2137=