Canonical Allele Identifier: CA1998806043
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108321342_108321344delinsCTG , CM000673.2:g.108321342_108321344delinsCTG GRCh38
NC_000011.9:g.108192069_108192071delinsCTG , CM000673.1:g.108192069_108192071delinsCTG GRCh37
NC_000011.8:g.107697279_107697281delinsCTG NCBI36
NG_009830.1:g.103511_103513delinsCTG , LRG_135:g.103511_103513delinsCTG
NG_054724.1:g.153489_153491delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.6494_6496delinsCTG (ATM) ENSP00000388058.2:p.Ser2165=
ENST00000713593.1:c.*5965_*5967delinsCTG (ATM) ENSP00000518889.1:n.*5965_*5967delinsCTG
ENST00000278616.9:c.6494_6496delinsCTG (ATM) ENSP00000278616.4:p.Ser2165=
ENST00000525056.2:n.913_915delinsCTG (ATM)
ENST00000682286.1:n.1251_1253delinsCTG (ATM)
ENST00000682302.1:n.912_914delinsCTG (ATM)
ENST00000683174.1:n.7978_7980delinsCTG (ATM)
ENST00000683524.1:n.1718_1720delinsCTG (ATM)
ENST00000684152.1:n.2208_2210delinsCTG (ATM)
ENST00000527805.6:c.*1558_*1560delinsCTG (ATM) ENSP00000435747.2:n.*1558_*1560delinsCTG
ENST00000675595.1:c.*1629_*1631delinsCTG (ATM) ENSP00000502563.1:n.*1629_*1631delinsCTG
ENST00000675843.1:c.6494_6496delinsCTG (ATM) MANE Select ENSP00000501606.1:p.Ser2165=
ENST00000278616.8:c.6494_6496delinsCTG (ATM) ENSP00000278616.4:p.Ser2165=
ENST00000452508.6:c.6494_6496delinsCTG (ATM) ENSP00000388058.2:p.Ser2165=
ENST00000524792.5:n.2709_2711delinsCTG (ATM)
ENST00000525729.5:c.641-12273_641-12271delinsCAG (C11orf65) ENSP00000433395.1:n.641-12273_641-12271de...
ENST00000533690.5:n.1898_1900delinsCTG (ATM)
NM_000051.3:c.6494_6496delinsCTG , LRG_135t1:c.6494_6496delinsCTG (ATM) NP_000042.3:p.Ser2165=
XM_005271561.3:c.6494_6496delinsCTG (ATM) XP_005271618.2:p.Ser2165=
XM_005271562.3:c.6494_6496delinsCTG (ATM) XP_005271619.2:p.Ser2165=
XM_006718843.2:c.6494_6496delinsCTG (ATM) XP_006718906.1:p.Ser2165=
XM_006718845.1:c.2450_2452delinsCTG (ATM) XP_006718908.1:p.Ser817=
XM_011542840.1:c.6494_6496delinsCTG (ATM) XP_011541142.1:p.Ser2165=
XM_011542841.1:c.6494_6496delinsCTG (ATM) XP_011541143.1:p.Ser2165=
XM_011542842.1:c.6329_6331delinsCTG (ATM) XP_011541144.1:p.Ser2110=
XM_011542843.1:c.6494_6496delinsCTG (ATM) XP_011541145.1:p.Ser2165=
XM_011542844.1:c.5450_5452delinsCTG (ATM) XP_011541146.1:p.Ser1817=
XM_011542845.1:c.5186_5188delinsCTG (ATM) XP_011541147.1:p.Ser1729=
XM_011542847.1:c.1565_1567delinsCTG (ATM) XP_011541149.1:p.Ser522=
NM_001330368.1:c.641-12273_641-12271delinsCAG (C11orf65) NP_001317297.1:n.641-12273_641-12271delin...
NM_001351110.1:c.*39-12273_*39-12271delinsCAG (C11orf65) NP_001338039.1:n.*39-12273_*39-12271delin...
NM_001351834.1:c.6494_6496delinsCTG (ATM) NP_001338763.1:p.Ser2165=
XM_005271562.5:c.6494_6496delinsCTG (ATM) XP_005271619.2:p.Ser2165=
XM_006718843.4:c.6494_6496delinsCTG (ATM) XP_006718906.1:p.Ser2165=
XM_006718845.2:c.2450_2452delinsCTG (ATM) XP_006718908.1:p.Ser817=
XM_011542840.3:c.6494_6496delinsCTG (ATM) XP_011541142.1:p.Ser2165=
XM_011542842.3:c.6329_6331delinsCTG (ATM) XP_011541144.1:p.Ser2110=
XM_011542843.2:c.6494_6496delinsCTG (ATM) XP_011541145.1:p.Ser2165=
XM_011542844.3:c.5450_5452delinsCTG (ATM) XP_011541146.1:p.Ser1817=
XM_011542845.2:c.5186_5188delinsCTG (ATM) XP_011541147.1:p.Ser1729=
XM_017017789.2:c.6494_6496delinsCTG (ATM) XP_016873278.1:p.Ser2165=
XM_017017790.2:c.6494_6496delinsCTG (ATM) XP_016873279.1:p.Ser2165=
NM_001330368.2:c.641-12273_641-12271delinsCAG (C11orf65) NP_001317297.1:n.641-12273_641-12271delin...
NM_001351110.2:c.*39-12273_*39-12271delinsCAG (C11orf65) NP_001338039.1:n.*39-12273_*39-12271delin...
NM_001351834.2:c.6494_6496delinsCTG (ATM) NP_001338763.1:p.Ser2165=
NM_000051.4:c.6494_6496delinsCTG (ATM) MANE Select NP_000042.3:p.Ser2165=