Canonical Allele Identifier: CA1998808534

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108330322_108330323delinsCT , CM000673.2:g.108330322_108330323delinsCT	GRCh38
NC_000011.9:g.108201049_108201050delinsCT , CM000673.1:g.108201049_108201050delinsCT	GRCh37
NC_000011.8:g.107706259_107706260delinsCT	NCBI36
NG_009830.1:g.112491_112492delinsCT , LRG_135:g.112491_112492delinsCT
NG_054724.1:g.144510_144511delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7416_7417delinsCT (ATM)	ENSP00000388058.2:p.Asn2472=
ENST00000713593.1:c.*6887_*6888delinsCT (ATM)	ENSP00000518889.1:n.*6887_*6888delinsCT
ENST00000278616.9:c.7416_7417delinsCT (ATM)	ENSP00000278616.4:p.Asn2472=
ENST00000525056.2:n.1835_1836delinsCT (ATM)
ENST00000525537.3:n.373_374delinsCT (ATM)
ENST00000638786.2:n.253_254delinsCT (ATM)
ENST00000682286.1:n.2173_2174delinsCT (ATM)
ENST00000682302.1:n.1834_1835delinsCT (ATM)
ENST00000683174.1:n.8900_8901delinsCT (ATM)
ENST00000683524.1:n.2640_2641delinsCT (ATM)
ENST00000684152.1:n.3130_3131delinsCT (ATM)
ENST00000684447.1:n.1879_1880delinsCT (ATM)
ENST00000527805.6:c.*2480_*2481delinsCT (ATM)	ENSP00000435747.2:n.*2480_*2481delinsCT
ENST00000675595.1:c.*2551_*2552delinsCT (ATM)	ENSP00000502563.1:n.*2551_*2552delinsCT
ENST00000675843.1:c.7416_7417delinsCT (ATM) MANE Select	ENSP00000501606.1:p.Asn2472=
ENST00000278616.8:c.7416_7417delinsCT (ATM)	ENSP00000278616.4:p.Asn2472=
ENST00000452508.6:c.7416_7417delinsCT (ATM)	ENSP00000388058.2:p.Asn2472=
ENST00000524792.5:n.3631_3632delinsCT (ATM)
ENST00000525729.5:c.641-21252_641-21251delinsAG (C11orf65)	ENSP00000433395.1:n.641-21252_641-21251delinsAG
ENST00000533690.5:n.2820_2821delinsCT (ATM)
NM_000051.3:c.7416_7417delinsCT , LRG_135t1:c.7416_7417delinsCT (ATM)	NP_000042.3:p.Asn2472=
XM_005271561.3:c.7416_7417delinsCT (ATM)	XP_005271618.2:p.Asn2472=
XM_005271562.3:c.7416_7417delinsCT (ATM)	XP_005271619.2:p.Asn2472=
XM_006718843.2:c.7416_7417delinsCT (ATM)	XP_006718906.1:p.Asn2472=
XM_006718845.1:c.3372_3373delinsCT (ATM)	XP_006718908.1:p.Asn1124=
XM_011542840.1:c.7416_7417delinsCT (ATM)	XP_011541142.1:p.Asn2472=
XM_011542841.1:c.7416_7417delinsCT (ATM)	XP_011541143.1:p.Asn2472=
XM_011542842.1:c.7251_7252delinsCT (ATM)	XP_011541144.1:p.Asn2417=
XM_011542843.1:c.7416_7417delinsCT (ATM)	XP_011541145.1:p.Asn2472=
XM_011542844.1:c.6372_6373delinsCT (ATM)	XP_011541146.1:p.Asn2124=
XM_011542845.1:c.6108_6109delinsCT (ATM)	XP_011541147.1:p.Asn2036=
XM_011542847.1:c.2487_2488delinsCT (ATM)	XP_011541149.1:p.Asn829=
NM_001330368.1:c.641-21252_641-21251delinsAG (C11orf65)	NP_001317297.1:n.641-21252_641-21251delinsAG
NM_001351110.1:c.*38+4897_*38+4898delinsAG (C11orf65)	NP_001338039.1:n.*38+4897_*38+4898delinsAG
NM_001351834.1:c.7416_7417delinsCT (ATM)	NP_001338763.1:p.Asn2472=
XM_005271562.5:c.7416_7417delinsCT (ATM)	XP_005271619.2:p.Asn2472=
XM_006718843.4:c.7416_7417delinsCT (ATM)	XP_006718906.1:p.Asn2472=
XM_006718845.2:c.3372_3373delinsCT (ATM)	XP_006718908.1:p.Asn1124=
XM_011542840.3:c.7416_7417delinsCT (ATM)	XP_011541142.1:p.Asn2472=
XM_011542842.3:c.7251_7252delinsCT (ATM)	XP_011541144.1:p.Asn2417=
XM_011542843.2:c.7416_7417delinsCT (ATM)	XP_011541145.1:p.Asn2472=
XM_011542844.3:c.6372_6373delinsCT (ATM)	XP_011541146.1:p.Asn2124=
XM_011542845.2:c.6108_6109delinsCT (ATM)	XP_011541147.1:p.Asn2036=
XM_017017789.2:c.7416_7417delinsCT (ATM)	XP_016873278.1:p.Asn2472=
XM_017017790.2:c.7416_7417delinsCT (ATM)	XP_016873279.1:p.Asn2472=
NM_001330368.2:c.641-21252_641-21251delinsAG (C11orf65)	NP_001317297.1:n.641-21252_641-21251delinsAG
NM_001351110.2:c.*38+4897_*38+4898delinsAG (C11orf65)	NP_001338039.1:n.*38+4897_*38+4898delinsAG
NM_001351834.2:c.7416_7417delinsCT (ATM)	NP_001338763.1:p.Asn2472=
NM_000051.4:c.7416_7417delinsCT (ATM) MANE Select	NP_000042.3:p.Asn2472=