Canonical Allele Identifier: CA1998811399

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108332899A= , CM000673.2:g.108332899A=	GRCh38
NC_000011.9:g.108203626A= , CM000673.1:g.108203626A=	GRCh37
NC_000011.8:g.107708836A=	NCBI36
NG_009830.1:g.115068A= , LRG_135:g.115068A=
NG_054724.1:g.141934T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7926A= (ATM)	ENSP00000388058.2:p.Arg2642=
ENST00000713593.1:c.*7397A= (ATM)	ENSP00000518889.1:n.*7397A=
ENST00000278616.9:c.7926A= (ATM)	ENSP00000278616.4:p.Arg2642=
ENST00000525056.2:n.2345A= (ATM)
ENST00000525537.3:n.1607A= (ATM)
ENST00000638786.2:n.625+862A= (ATM)
ENST00000682286.1:n.2683A= (ATM)
ENST00000682302.1:n.2344A= (ATM)
ENST00000683174.1:n.9410A= (ATM)
ENST00000683524.1:n.3150A= (ATM)
ENST00000684152.1:n.3344-987A= (ATM)
ENST00000684180.1:n.400A= (ATM)
ENST00000684447.1:n.3434A= (ATM)
ENST00000527805.6:c.*2990A= (ATM)	ENSP00000435747.2:n.*2990A=
ENST00000675595.1:c.*3061A= (ATM)	ENSP00000502563.1:n.*3061A=
ENST00000675843.1:c.7926A= (ATM) MANE Select	ENSP00000501606.1:p.Arg2642=
ENST00000278616.8:c.7926A= (ATM)	ENSP00000278616.4:p.Arg2642=
ENST00000452508.6:c.7926A= (ATM)	ENSP00000388058.2:p.Arg2642=
ENST00000524755.5:c.300-1332T= (C11orf65)
ENST00000524792.5:n.4141A= (ATM)
ENST00000525056.1:n.123A= (ATM)
ENST00000525729.5:c.641-23828T= (C11orf65)	ENSP00000433395.1:n.641-23828T=
ENST00000527531.5:c.*1270-1332T= (C11orf65)	ENSP00000431706.1:n.*1270-1332T=
ENST00000533690.5:n.3330A= (ATM)
ENST00000533979.5:n.138A= (ATM)
ENST00000615746.4:c.*1270-1332T= (C11orf65)	ENSP00000483537.1:n.*1270-1332T=
NM_000051.3:c.7926A= , LRG_135t1:c.7926A= (ATM)	NP_000042.3:p.Arg2642=
XM_005271414.3:c.*39-1332T= (C11orf65)	XP_005271471.1:n.*39-1332T=
XM_005271415.3:c.805-1332T= (C11orf65)	XP_005271472.1:n.805-1332T=
XM_005271561.3:c.7926A= (ATM)	XP_005271618.2:p.Arg2642=
XM_005271562.3:c.7926A= (ATM)	XP_005271619.2:p.Arg2642=
XM_006718843.2:c.7926A= (ATM)	XP_006718906.1:p.Arg2642=
XM_006718845.1:c.3882A= (ATM)	XP_006718908.1:p.Arg1294=
XM_011542840.1:c.7926A= (ATM)	XP_011541142.1:p.Arg2642=
XM_011542841.1:c.7926A= (ATM)	XP_011541143.1:p.Arg2642=
XM_011542842.1:c.7761A= (ATM)	XP_011541144.1:p.Arg2587=
XM_011542843.1:c.7926A= (ATM)	XP_011541145.1:p.Arg2642=
XM_011542844.1:c.6882A= (ATM)	XP_011541146.1:p.Arg2294=
XM_011542845.1:c.6618A= (ATM)	XP_011541147.1:p.Arg2206=
XM_011542847.1:c.2997A= (ATM)	XP_011541149.1:p.Arg999=
NM_001330368.1:c.641-23828T= (C11orf65)	NP_001317297.1:n.641-23828T=
NM_001351110.1:c.*38+2321T= (C11orf65)	NP_001338039.1:n.*38+2321T=
NM_001351834.1:c.7926A= (ATM)	NP_001338763.1:p.Arg2642=
NR_147053.2:n.2375-1332T= (C11orf65)
XM_005271414.4:c.*39-1332T= (C11orf65)	XP_005271471.1:n.*39-1332T=
XM_005271415.4:c.805-1332T= (C11orf65)	XP_005271472.1:n.805-1332T=
XM_005271562.5:c.7926A= (ATM)	XP_005271619.2:p.Arg2642=
XM_006718843.4:c.7926A= (ATM)	XP_006718906.1:p.Arg2642=
XM_006718845.2:c.3882A= (ATM)	XP_006718908.1:p.Arg1294=
XM_011542840.3:c.7926A= (ATM)	XP_011541142.1:p.Arg2642=
XM_011542842.3:c.7761A= (ATM)	XP_011541144.1:p.Arg2587=
XM_011542843.2:c.7926A= (ATM)	XP_011541145.1:p.Arg2642=
XM_011542844.3:c.6882A= (ATM)	XP_011541146.1:p.Arg2294=
XM_011542845.2:c.6618A= (ATM)	XP_011541147.1:p.Arg2206=
XM_017017789.2:c.7926A= (ATM)	XP_016873278.1:p.Arg2642=
XM_017017790.2:c.7926A= (ATM)	XP_016873279.1:p.Arg2642=
NM_001330368.2:c.641-23828T= (C11orf65)	NP_001317297.1:n.641-23828T=
NM_001351110.2:c.*38+2321T= (C11orf65)	NP_001338039.1:n.*38+2321T=
NM_001351834.2:c.7926A= (ATM)	NP_001338763.1:p.Arg2642=
NM_000051.4:c.7926A= (ATM) MANE Select	NP_000042.3:p.Arg2642=
NR_147053.3:n.2373-1332T= (C11orf65)