Canonical Allele Identifier: CA1998809718

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327754A= , CM000673.2:g.108327754A=	GRCh38
NC_000011.9:g.108198481A= , CM000673.1:g.108198481A=	GRCh37
NC_000011.8:g.107703691A=	NCBI36
NG_009830.1:g.109923A= , LRG_135:g.109923A=
NG_054724.1:g.147079T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7085A= (ATM)	ENSP00000388058.2:p.Glu2362=
ENST00000713593.1:c.*6556A= (ATM)	ENSP00000518889.1:n.*6556A=
ENST00000278616.9:c.7085A= (ATM)	ENSP00000278616.4:p.Glu2362=
ENST00000525056.2:n.1504A= (ATM)
ENST00000525537.3:n.42A= (ATM)
ENST00000682286.1:n.1842A= (ATM)
ENST00000682302.1:n.1503A= (ATM)
ENST00000683174.1:n.8569A= (ATM)
ENST00000683524.1:n.2309A= (ATM)
ENST00000684152.1:n.2799A= (ATM)
ENST00000684447.1:n.1548A= (ATM)
ENST00000527805.6:c.*2149A= (ATM)	ENSP00000435747.2:n.*2149A=
ENST00000675595.1:c.*2220A= (ATM)	ENSP00000502563.1:n.*2220A=
ENST00000675843.1:c.7085A= (ATM) MANE Select	ENSP00000501606.1:p.Glu2362=
ENST00000278616.8:c.7085A= (ATM)	ENSP00000278616.4:p.Glu2362=
ENST00000452508.6:c.7085A= (ATM)	ENSP00000388058.2:p.Glu2362=
ENST00000524792.5:n.3300A= (ATM)
ENST00000525537.2:n.361A= (ATM)
ENST00000525729.5:c.641-18683T= (C11orf65)	ENSP00000433395.1:n.641-18683T=
ENST00000527389.2:n.110A= (ATM)
ENST00000533690.5:n.2489A= (ATM)
NM_000051.3:c.7085A= , LRG_135t1:c.7085A= (ATM)	NP_000042.3:p.Glu2362=
XM_005271561.3:c.7085A= (ATM)	XP_005271618.2:p.Glu2362=
XM_005271562.3:c.7085A= (ATM)	XP_005271619.2:p.Glu2362=
XM_006718843.2:c.7085A= (ATM)	XP_006718906.1:p.Glu2362=
XM_006718845.1:c.3041A= (ATM)	XP_006718908.1:p.Glu1014=
XM_011542840.1:c.7085A= (ATM)	XP_011541142.1:p.Glu2362=
XM_011542841.1:c.7085A= (ATM)	XP_011541143.1:p.Glu2362=
XM_011542842.1:c.6920A= (ATM)	XP_011541144.1:p.Glu2307=
XM_011542843.1:c.7085A= (ATM)	XP_011541145.1:p.Glu2362=
XM_011542844.1:c.6041A= (ATM)	XP_011541146.1:p.Glu2014=
XM_011542845.1:c.5777A= (ATM)	XP_011541147.1:p.Glu1926=
XM_011542847.1:c.2156A= (ATM)	XP_011541149.1:p.Glu719=
NM_001330368.1:c.641-18683T= (C11orf65)	NP_001317297.1:n.641-18683T=
NM_001351110.1:c.*38+7466T= (C11orf65)	NP_001338039.1:n.*38+7466T=
NM_001351834.1:c.7085A= (ATM)	NP_001338763.1:p.Glu2362=
XM_005271562.5:c.7085A= (ATM)	XP_005271619.2:p.Glu2362=
XM_006718843.4:c.7085A= (ATM)	XP_006718906.1:p.Glu2362=
XM_006718845.2:c.3041A= (ATM)	XP_006718908.1:p.Glu1014=
XM_011542840.3:c.7085A= (ATM)	XP_011541142.1:p.Glu2362=
XM_011542842.3:c.6920A= (ATM)	XP_011541144.1:p.Glu2307=
XM_011542843.2:c.7085A= (ATM)	XP_011541145.1:p.Glu2362=
XM_011542844.3:c.6041A= (ATM)	XP_011541146.1:p.Glu2014=
XM_011542845.2:c.5777A= (ATM)	XP_011541147.1:p.Glu1926=
XM_017017789.2:c.7085A= (ATM)	XP_016873278.1:p.Glu2362=
XM_017017790.2:c.7085A= (ATM)	XP_016873279.1:p.Glu2362=
NM_001330368.2:c.641-18683T= (C11orf65)	NP_001317297.1:n.641-18683T=
NM_001351110.2:c.*38+7466T= (C11orf65)	NP_001338039.1:n.*38+7466T=
NM_001351834.2:c.7085A= (ATM)	NP_001338763.1:p.Glu2362=
NM_000051.4:c.7085A= (ATM) MANE Select	NP_000042.3:p.Glu2362=