Canonical Allele Identifier: CA1998811374

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108332854T= , CM000673.2:g.108332854T=	GRCh38
NC_000011.9:g.108203581T= , CM000673.1:g.108203581T=	GRCh37
NC_000011.8:g.107708791T=	NCBI36
NG_009830.1:g.115023T= , LRG_135:g.115023T=
NG_054724.1:g.141979A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7881T= (ATM)	ENSP00000388058.2:p.Tyr2627=
ENST00000713593.1:c.*7352T= (ATM)	ENSP00000518889.1:n.*7352T=
ENST00000278616.9:c.7881T= (ATM)	ENSP00000278616.4:p.Tyr2627=
ENST00000525056.2:n.2300T= (ATM)
ENST00000525537.3:n.1562T= (ATM)
ENST00000638786.2:n.625+817T= (ATM)
ENST00000682286.1:n.2638T= (ATM)
ENST00000682302.1:n.2299T= (ATM)
ENST00000683174.1:n.9365T= (ATM)
ENST00000683524.1:n.3105T= (ATM)
ENST00000684152.1:n.3344-1032T= (ATM)
ENST00000684180.1:n.355T= (ATM)
ENST00000684447.1:n.3389T= (ATM)
ENST00000527805.6:c.*2945T= (ATM)	ENSP00000435747.2:n.*2945T=
ENST00000675595.1:c.*3016T= (ATM)	ENSP00000502563.1:n.*3016T=
ENST00000675843.1:c.7881T= (ATM) MANE Select	ENSP00000501606.1:p.Tyr2627=
ENST00000278616.8:c.7881T= (ATM)	ENSP00000278616.4:p.Tyr2627=
ENST00000452508.6:c.7881T= (ATM)	ENSP00000388058.2:p.Tyr2627=
ENST00000524755.5:c.300-1287A= (C11orf65)
ENST00000524792.5:n.4096T= (ATM)
ENST00000525056.1:n.78T= (ATM)
ENST00000525729.5:c.641-23783A= (C11orf65)	ENSP00000433395.1:n.641-23783A=
ENST00000527531.5:c.*1270-1287A= (C11orf65)	ENSP00000431706.1:n.*1270-1287A=
ENST00000533690.5:n.3285T= (ATM)
ENST00000533979.5:n.93T= (ATM)
ENST00000615746.4:c.*1270-1287A= (C11orf65)	ENSP00000483537.1:n.*1270-1287A=
NM_000051.3:c.7881T= , LRG_135t1:c.7881T= (ATM)	NP_000042.3:p.Tyr2627=
XM_005271414.3:c.*39-1287A= (C11orf65)	XP_005271471.1:n.*39-1287A=
XM_005271415.3:c.805-1287A= (C11orf65)	XP_005271472.1:n.805-1287A=
XM_005271561.3:c.7881T= (ATM)	XP_005271618.2:p.Tyr2627=
XM_005271562.3:c.7881T= (ATM)	XP_005271619.2:p.Tyr2627=
XM_006718843.2:c.7881T= (ATM)	XP_006718906.1:p.Tyr2627=
XM_006718845.1:c.3837T= (ATM)	XP_006718908.1:p.Tyr1279=
XM_011542840.1:c.7881T= (ATM)	XP_011541142.1:p.Tyr2627=
XM_011542841.1:c.7881T= (ATM)	XP_011541143.1:p.Tyr2627=
XM_011542842.1:c.7716T= (ATM)	XP_011541144.1:p.Tyr2572=
XM_011542843.1:c.7881T= (ATM)	XP_011541145.1:p.Tyr2627=
XM_011542844.1:c.6837T= (ATM)	XP_011541146.1:p.Tyr2279=
XM_011542845.1:c.6573T= (ATM)	XP_011541147.1:p.Tyr2191=
XM_011542847.1:c.2952T= (ATM)	XP_011541149.1:p.Tyr984=
NM_001330368.1:c.641-23783A= (C11orf65)	NP_001317297.1:n.641-23783A=
NM_001351110.1:c.*38+2366A= (C11orf65)	NP_001338039.1:n.*38+2366A=
NM_001351834.1:c.7881T= (ATM)	NP_001338763.1:p.Tyr2627=
NR_147053.2:n.2375-1287A= (C11orf65)
XM_005271414.4:c.*39-1287A= (C11orf65)	XP_005271471.1:n.*39-1287A=
XM_005271415.4:c.805-1287A= (C11orf65)	XP_005271472.1:n.805-1287A=
XM_005271562.5:c.7881T= (ATM)	XP_005271619.2:p.Tyr2627=
XM_006718843.4:c.7881T= (ATM)	XP_006718906.1:p.Tyr2627=
XM_006718845.2:c.3837T= (ATM)	XP_006718908.1:p.Tyr1279=
XM_011542840.3:c.7881T= (ATM)	XP_011541142.1:p.Tyr2627=
XM_011542842.3:c.7716T= (ATM)	XP_011541144.1:p.Tyr2572=
XM_011542843.2:c.7881T= (ATM)	XP_011541145.1:p.Tyr2627=
XM_011542844.3:c.6837T= (ATM)	XP_011541146.1:p.Tyr2279=
XM_011542845.2:c.6573T= (ATM)	XP_011541147.1:p.Tyr2191=
XM_017017789.2:c.7881T= (ATM)	XP_016873278.1:p.Tyr2627=
XM_017017790.2:c.7881T= (ATM)	XP_016873279.1:p.Tyr2627=
NM_001330368.2:c.641-23783A= (C11orf65)	NP_001317297.1:n.641-23783A=
NM_001351110.2:c.*38+2366A= (C11orf65)	NP_001338039.1:n.*38+2366A=
NM_001351834.2:c.7881T= (ATM)	NP_001338763.1:p.Tyr2627=
NM_000051.4:c.7881T= (ATM) MANE Select	NP_000042.3:p.Tyr2627=
NR_147053.3:n.2373-1287A= (C11orf65)