Canonical Allele Identifier: CA1998810516
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108329027G= , CM000673.2:g.108329027G= GRCh38
NC_000011.9:g.108199754G= , CM000673.1:g.108199754G= GRCh37
NC_000011.8:g.107704964G= NCBI36
NG_009830.1:g.111196G= , LRG_135:g.111196G=
NG_054724.1:g.145806C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.7096G= (ATM) ENSP00000388058.2:p.Glu2366=
ENST00000713593.1:c.*6567G= (ATM) ENSP00000518889.1:n.*6567G=
ENST00000278616.9:c.7096G= (ATM) ENSP00000278616.4:p.Glu2366=
ENST00000525056.2:n.1515G= (ATM)
ENST00000525537.3:n.53G= (ATM)
ENST00000682286.1:n.1853G= (ATM)
ENST00000682302.1:n.1514G= (ATM)
ENST00000683174.1:n.8580G= (ATM)
ENST00000683524.1:n.2320G= (ATM)
ENST00000684152.1:n.2810G= (ATM)
ENST00000684447.1:n.1559G= (ATM)
ENST00000527805.6:c.*2160G= (ATM) ENSP00000435747.2:n.*2160G=
ENST00000675595.1:c.*2231G= (ATM) ENSP00000502563.1:n.*2231G=
ENST00000675843.1:c.7096G= (ATM) MANE Select ENSP00000501606.1:p.Glu2366=
ENST00000278616.8:c.7096G= (ATM) ENSP00000278616.4:p.Glu2366=
ENST00000452508.6:c.7096G= (ATM) ENSP00000388058.2:p.Glu2366=
ENST00000524792.5:n.3311G= (ATM)
ENST00000525537.2:n.372G= (ATM)
ENST00000525729.5:c.641-19956C= (C11orf65) ENSP00000433395.1:n.641-19956C=
ENST00000527389.2:n.121G= (ATM)
ENST00000533690.5:n.2500G= (ATM)
NM_000051.3:c.7096G= , LRG_135t1:c.7096G= (ATM) NP_000042.3:p.Glu2366=
XM_005271561.3:c.7096G= (ATM) XP_005271618.2:p.Glu2366=
XM_005271562.3:c.7096G= (ATM) XP_005271619.2:p.Glu2366=
XM_006718843.2:c.7096G= (ATM) XP_006718906.1:p.Glu2366=
XM_006718845.1:c.3052G= (ATM) XP_006718908.1:p.Glu1018=
XM_011542840.1:c.7096G= (ATM) XP_011541142.1:p.Glu2366=
XM_011542841.1:c.7096G= (ATM) XP_011541143.1:p.Glu2366=
XM_011542842.1:c.6931G= (ATM) XP_011541144.1:p.Glu2311=
XM_011542843.1:c.7096G= (ATM) XP_011541145.1:p.Glu2366=
XM_011542844.1:c.6052G= (ATM) XP_011541146.1:p.Glu2018=
XM_011542845.1:c.5788G= (ATM) XP_011541147.1:p.Glu1930=
XM_011542847.1:c.2167G= (ATM) XP_011541149.1:p.Glu723=
NM_001330368.1:c.641-19956C= (C11orf65) NP_001317297.1:n.641-19956C=
NM_001351110.1:c.*38+6193C= (C11orf65) NP_001338039.1:n.*38+6193C=
NM_001351834.1:c.7096G= (ATM) NP_001338763.1:p.Glu2366=
XM_005271562.5:c.7096G= (ATM) XP_005271619.2:p.Glu2366=
XM_006718843.4:c.7096G= (ATM) XP_006718906.1:p.Glu2366=
XM_006718845.2:c.3052G= (ATM) XP_006718908.1:p.Glu1018=
XM_011542840.3:c.7096G= (ATM) XP_011541142.1:p.Glu2366=
XM_011542842.3:c.6931G= (ATM) XP_011541144.1:p.Glu2311=
XM_011542843.2:c.7096G= (ATM) XP_011541145.1:p.Glu2366=
XM_011542844.3:c.6052G= (ATM) XP_011541146.1:p.Glu2018=
XM_011542845.2:c.5788G= (ATM) XP_011541147.1:p.Glu1930=
XM_017017789.2:c.7096G= (ATM) XP_016873278.1:p.Glu2366=
XM_017017790.2:c.7096G= (ATM) XP_016873279.1:p.Glu2366=
NM_001330368.2:c.641-19956C= (C11orf65) NP_001317297.1:n.641-19956C=
NM_001351110.2:c.*38+6193C= (C11orf65) NP_001338039.1:n.*38+6193C=
NM_001351834.2:c.7096G= (ATM) NP_001338763.1:p.Glu2366=
NM_000051.4:c.7096G= (ATM) MANE Select NP_000042.3:p.Glu2366=