Canonical Allele Identifier: CA2580083133

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 2431274
• ClinVar RCV Id: RCV003140334

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108326139dup , CM000673.2:g.108326139dup	GRCh38
NC_000011.9:g.108196866dup , CM000673.1:g.108196866dup	GRCh37
NC_000011.8:g.107702076dup	NCBI36
NG_009830.1:g.108308dup , LRG_135:g.108308dup
NG_054724.1:g.148694dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6889dup (ATM)	ENSP00000388058.2:p.Gln2297ProfsTer?
ENST00000713593.1:c.*6360dup (ATM)	ENSP00000518889.1:n.*6360dup
ENST00000278616.9:c.6889dup (ATM)	ENSP00000278616.4:p.Gln2297ProfsTer?
ENST00000525056.2:n.1308dup (ATM)
ENST00000682286.1:n.1646dup (ATM)
ENST00000682302.1:n.1307dup (ATM)
ENST00000683174.1:n.8373dup (ATM)
ENST00000683524.1:n.2113dup (ATM)
ENST00000684152.1:n.2603dup (ATM)
ENST00000527805.6:c.*1953dup (ATM)	ENSP00000435747.2:n.*1953dup
ENST00000675595.1:c.*2024dup (ATM)	ENSP00000502563.1:n.*2024dup
ENST00000675843.1:c.6889dup (ATM) MANE Select	ENSP00000501606.1:p.Gln2297ProfsTer?
ENST00000278616.8:c.6889dup (ATM)	ENSP00000278616.4:p.Gln2297ProfsTer?
ENST00000452508.6:c.6889dup (ATM)	ENSP00000388058.2:p.Gln2297ProfsTer?
ENST00000524792.5:n.3104dup (ATM)
ENST00000525729.5:c.641-17068dup (C11orf65)	ENSP00000433395.1:n.641-17068dup
ENST00000533690.5:n.2293dup (ATM)
NM_000051.3:c.6889dup , LRG_135t1:c.6889dup (ATM)	NP_000042.3:p.Gln2297ProfsTer?
XM_005271561.3:c.6889dup (ATM)	XP_005271618.2:p.Gln2297ProfsTer?
XM_005271562.3:c.6889dup (ATM)	XP_005271619.2:p.Gln2297ProfsTer?
XM_006718843.2:c.6889dup (ATM)	XP_006718906.1:p.Gln2297ProfsTer?
XM_006718845.1:c.2845dup (ATM)	XP_006718908.1:p.Gln949ProfsTer?
XM_011542840.1:c.6889dup (ATM)	XP_011541142.1:p.Gln2297ProfsTer?
XM_011542841.1:c.6889dup (ATM)	XP_011541143.1:p.Gln2297ProfsTer?
XM_011542842.1:c.6724dup (ATM)	XP_011541144.1:p.Gln2242ProfsTer?
XM_011542843.1:c.6889dup (ATM)	XP_011541145.1:p.Gln2297ProfsTer?
XM_011542844.1:c.5845dup (ATM)	XP_011541146.1:p.Gln1949ProfsTer?
XM_011542845.1:c.5581dup (ATM)	XP_011541147.1:p.Gln1861ProfsTer?
XM_011542847.1:c.1960dup (ATM)	XP_011541149.1:p.Gln654ProfsTer?
NM_001330368.1:c.641-17068dup (C11orf65)	NP_001317297.1:n.641-17068dup
NM_001351110.1:c.*38+9081dup (C11orf65)	NP_001338039.1:n.*38+9081dup
NM_001351834.1:c.6889dup (ATM)	NP_001338763.1:p.Gln2297ProfsTer?
XM_005271562.5:c.6889dup (ATM)	XP_005271619.2:p.Gln2297ProfsTer?
XM_006718843.4:c.6889dup (ATM)	XP_006718906.1:p.Gln2297ProfsTer?
XM_006718845.2:c.2845dup (ATM)	XP_006718908.1:p.Gln949ProfsTer?
XM_011542840.3:c.6889dup (ATM)	XP_011541142.1:p.Gln2297ProfsTer?
XM_011542842.3:c.6724dup (ATM)	XP_011541144.1:p.Gln2242ProfsTer?
XM_011542843.2:c.6889dup (ATM)	XP_011541145.1:p.Gln2297ProfsTer?
XM_011542844.3:c.5845dup (ATM)	XP_011541146.1:p.Gln1949ProfsTer?
XM_011542845.2:c.5581dup (ATM)	XP_011541147.1:p.Gln1861ProfsTer?
XM_017017789.2:c.6889dup (ATM)	XP_016873278.1:p.Gln2297ProfsTer?
XM_017017790.2:c.6889dup (ATM)	XP_016873279.1:p.Gln2297ProfsTer?
NM_001330368.2:c.641-17068dup (C11orf65)	NP_001317297.1:n.641-17068dup
NM_001351110.2:c.*38+9081dup (C11orf65)	NP_001338039.1:n.*38+9081dup
NM_001351834.2:c.6889dup (ATM)	NP_001338763.1:p.Gln2297ProfsTer?
NM_000051.4:c.6889dup (ATM) MANE Select	NP_000042.3:p.Gln2297ProfsTer?