Canonical Allele Identifier: CA1998809784

Gene: ATM C11orf65

Linked Data

• dbSNP Id: rs2085841594

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327867dup , CM000673.2:g.108327867dup	GRCh38
NC_000011.9:g.108198594dup , CM000673.1:g.108198594dup	GRCh37
NC_000011.8:g.107703804dup	NCBI36
NG_009830.1:g.110036dup , LRG_135:g.110036dup
NG_054724.1:g.146970dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7089+109dup (ATM)	ENSP00000388058.2:n.7089+109dup
ENST00000713593.1:c.*6560+109dup (ATM)	ENSP00000518889.1:n.*6560+109dup
ENST00000278616.9:c.7089+109dup (ATM)	ENSP00000278616.4:n.7089+109dup
ENST00000525056.2:n.1508+109dup (ATM)
ENST00000525537.3:n.46+109dup (ATM)
ENST00000682286.1:n.1846+109dup (ATM)
ENST00000682302.1:n.1507+109dup (ATM)
ENST00000683174.1:n.8573+109dup (ATM)
ENST00000683524.1:n.2313+109dup (ATM)
ENST00000684152.1:n.2803+109dup (ATM)
ENST00000684447.1:n.1552+109dup (ATM)
ENST00000527805.6:c.*2153+109dup (ATM)	ENSP00000435747.2:n.*2153+109dup
ENST00000675595.1:c.*2224+109dup (ATM)	ENSP00000502563.1:n.*2224+109dup
ENST00000675843.1:c.7089+109dup (ATM) MANE Select	ENSP00000501606.1:n.7089+109dup
ENST00000278616.8:c.7089+109dup (ATM)	ENSP00000278616.4:n.7089+109dup
ENST00000452508.6:c.7089+109dup (ATM)	ENSP00000388058.2:n.7089+109dup
ENST00000524792.5:n.3304+109dup (ATM)
ENST00000525537.2:n.365+109dup (ATM)
ENST00000525729.5:c.641-18792dup (C11orf65)	ENSP00000433395.1:n.641-18792dup
ENST00000527389.2:n.114+109dup (ATM)
ENST00000533690.5:n.2493+109dup (ATM)
NM_000051.3:c.7089+109dup , LRG_135t1:c.7089+109dup (ATM)	NP_000042.3:n.7089+109dup
XM_005271561.3:c.7089+109dup (ATM)	XP_005271618.2:n.7089+109dup
XM_005271562.3:c.7089+109dup (ATM)	XP_005271619.2:n.7089+109dup
XM_006718843.2:c.7089+109dup (ATM)	XP_006718906.1:n.7089+109dup
XM_006718845.1:c.3045+109dup (ATM)	XP_006718908.1:n.3045+109dup
XM_011542840.1:c.7089+109dup (ATM)	XP_011541142.1:n.7089+109dup
XM_011542841.1:c.7089+109dup (ATM)	XP_011541143.1:n.7089+109dup
XM_011542842.1:c.6924+109dup (ATM)	XP_011541144.1:n.6924+109dup
XM_011542843.1:c.7089+109dup (ATM)	XP_011541145.1:n.7089+109dup
XM_011542844.1:c.6045+109dup (ATM)	XP_011541146.1:n.6045+109dup
XM_011542845.1:c.5781+109dup (ATM)	XP_011541147.1:n.5781+109dup
XM_011542847.1:c.2160+109dup (ATM)	XP_011541149.1:n.2160+109dup
NM_001330368.1:c.641-18792dup (C11orf65)	NP_001317297.1:n.641-18792dup
NM_001351110.1:c.*38+7357dup (C11orf65)	NP_001338039.1:n.*38+7357dup
NM_001351834.1:c.7089+109dup (ATM)	NP_001338763.1:n.7089+109dup
XM_005271562.5:c.7089+109dup (ATM)	XP_005271619.2:n.7089+109dup
XM_006718843.4:c.7089+109dup (ATM)	XP_006718906.1:n.7089+109dup
XM_006718845.2:c.3045+109dup (ATM)	XP_006718908.1:n.3045+109dup
XM_011542840.3:c.7089+109dup (ATM)	XP_011541142.1:n.7089+109dup
XM_011542842.3:c.6924+109dup (ATM)	XP_011541144.1:n.6924+109dup
XM_011542843.2:c.7089+109dup (ATM)	XP_011541145.1:n.7089+109dup
XM_011542844.3:c.6045+109dup (ATM)	XP_011541146.1:n.6045+109dup
XM_011542845.2:c.5781+109dup (ATM)	XP_011541147.1:n.5781+109dup
XM_017017789.2:c.7089+109dup (ATM)	XP_016873278.1:n.7089+109dup
XM_017017790.2:c.7089+109dup (ATM)	XP_016873279.1:n.7089+109dup
NM_001330368.2:c.641-18792dup (C11orf65)	NP_001317297.1:n.641-18792dup
NM_001351110.2:c.*38+7357dup (C11orf65)	NP_001338039.1:n.*38+7357dup
NM_001351834.2:c.7089+109dup (ATM)	NP_001338763.1:n.7089+109dup
NM_000051.4:c.7089+109dup (ATM) MANE Select	NP_000042.3:n.7089+109dup