Canonical Allele Identifier: CA1998808512
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108330308G= , CM000673.2:g.108330308G= GRCh38
NC_000011.9:g.108201035G= , CM000673.1:g.108201035G= GRCh37
NC_000011.8:g.107706245G= NCBI36
NG_009830.1:g.112477G= , LRG_135:g.112477G=
NG_054724.1:g.144525C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.7402G= (ATM) ENSP00000388058.2:p.Glu2468=
ENST00000713593.1:c.*6873G= (ATM) ENSP00000518889.1:n.*6873G=
ENST00000278616.9:c.7402G= (ATM) ENSP00000278616.4:p.Glu2468=
ENST00000525056.2:n.1821G= (ATM)
ENST00000525537.3:n.359G= (ATM)
ENST00000638786.2:n.239G= (ATM)
ENST00000682286.1:n.2159G= (ATM)
ENST00000682302.1:n.1820G= (ATM)
ENST00000683174.1:n.8886G= (ATM)
ENST00000683524.1:n.2626G= (ATM)
ENST00000684152.1:n.3116G= (ATM)
ENST00000684447.1:n.1865G= (ATM)
ENST00000527805.6:c.*2466G= (ATM) ENSP00000435747.2:n.*2466G=
ENST00000675595.1:c.*2537G= (ATM) ENSP00000502563.1:n.*2537G=
ENST00000675843.1:c.7402G= (ATM) MANE Select ENSP00000501606.1:p.Glu2468=
ENST00000278616.8:c.7402G= (ATM) ENSP00000278616.4:p.Glu2468=
ENST00000452508.6:c.7402G= (ATM) ENSP00000388058.2:p.Glu2468=
ENST00000524792.5:n.3617G= (ATM)
ENST00000525729.5:c.641-21237C= (C11orf65) ENSP00000433395.1:n.641-21237C=
ENST00000533690.5:n.2806G= (ATM)
NM_000051.3:c.7402G= , LRG_135t1:c.7402G= (ATM) NP_000042.3:p.Glu2468=
XM_005271561.3:c.7402G= (ATM) XP_005271618.2:p.Glu2468=
XM_005271562.3:c.7402G= (ATM) XP_005271619.2:p.Glu2468=
XM_006718843.2:c.7402G= (ATM) XP_006718906.1:p.Glu2468=
XM_006718845.1:c.3358G= (ATM) XP_006718908.1:p.Glu1120=
XM_011542840.1:c.7402G= (ATM) XP_011541142.1:p.Glu2468=
XM_011542841.1:c.7402G= (ATM) XP_011541143.1:p.Glu2468=
XM_011542842.1:c.7237G= (ATM) XP_011541144.1:p.Glu2413=
XM_011542843.1:c.7402G= (ATM) XP_011541145.1:p.Glu2468=
XM_011542844.1:c.6358G= (ATM) XP_011541146.1:p.Glu2120=
XM_011542845.1:c.6094G= (ATM) XP_011541147.1:p.Glu2032=
XM_011542847.1:c.2473G= (ATM) XP_011541149.1:p.Glu825=
NM_001330368.1:c.641-21237C= (C11orf65) NP_001317297.1:n.641-21237C=
NM_001351110.1:c.*38+4912C= (C11orf65) NP_001338039.1:n.*38+4912C=
NM_001351834.1:c.7402G= (ATM) NP_001338763.1:p.Glu2468=
XM_005271562.5:c.7402G= (ATM) XP_005271619.2:p.Glu2468=
XM_006718843.4:c.7402G= (ATM) XP_006718906.1:p.Glu2468=
XM_006718845.2:c.3358G= (ATM) XP_006718908.1:p.Glu1120=
XM_011542840.3:c.7402G= (ATM) XP_011541142.1:p.Glu2468=
XM_011542842.3:c.7237G= (ATM) XP_011541144.1:p.Glu2413=
XM_011542843.2:c.7402G= (ATM) XP_011541145.1:p.Glu2468=
XM_011542844.3:c.6358G= (ATM) XP_011541146.1:p.Glu2120=
XM_011542845.2:c.6094G= (ATM) XP_011541147.1:p.Glu2032=
XM_017017789.2:c.7402G= (ATM) XP_016873278.1:p.Glu2468=
XM_017017790.2:c.7402G= (ATM) XP_016873279.1:p.Glu2468=
NM_001330368.2:c.641-21237C= (C11orf65) NP_001317297.1:n.641-21237C=
NM_001351110.2:c.*38+4912C= (C11orf65) NP_001338039.1:n.*38+4912C=
NM_001351834.2:c.7402G= (ATM) NP_001338763.1:p.Glu2468=
NM_000051.4:c.7402G= (ATM) MANE Select NP_000042.3:p.Glu2468=