Canonical Allele Identifier: CA2580083172

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 1756646
• ClinVar RCV Id: RCV002378245

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327671del , CM000673.2:g.108327671del	GRCh38
NC_000011.9:g.108198398del , CM000673.1:g.108198398del	GRCh37
NC_000011.8:g.107703608del	NCBI36
NG_009830.1:g.109840del , LRG_135:g.109840del
NG_054724.1:g.147162del

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.7002del (ATM)	ENSP00000388058.2:p.Tyr2334Ter
ENST00000713593.1:c.*6473del (ATM)	ENSP00000518889.1:n.*6473del
ENST00000278616.9:c.7002del (ATM)	ENSP00000278616.4:p.Tyr2334Ter
ENST00000525056.2:n.1421del (ATM)
ENST00000682286.1:n.1759del (ATM)
ENST00000682302.1:n.1420del (ATM)
ENST00000683174.1:n.8486del (ATM)
ENST00000683524.1:n.2226del (ATM)
ENST00000684152.1:n.2716del (ATM)
ENST00000684447.1:n.1465del (ATM)
ENST00000527805.6:c.*2066del (ATM)	ENSP00000435747.2:n.*2066del
ENST00000675595.1:c.*2137del (ATM)	ENSP00000502563.1:n.*2137del
ENST00000675843.1:c.7002del (ATM) MANE Select	ENSP00000501606.1:p.Tyr2334Ter
ENST00000278616.8:c.7002del (ATM)	ENSP00000278616.4:p.Tyr2334Ter
ENST00000452508.6:c.7002del (ATM)	ENSP00000388058.2:p.Tyr2334Ter
ENST00000524792.5:n.3217del (ATM)
ENST00000525537.2:n.278del (ATM)
ENST00000525729.5:c.641-18600del (C11orf65)	ENSP00000433395.1:n.641-18600del
ENST00000527389.2:n.27del (ATM)
ENST00000533690.5:n.2406del (ATM)
NM_000051.3:c.7002del , LRG_135t1:c.7002del (ATM)	NP_000042.3:p.Tyr2334Ter
XM_005271561.3:c.7002del (ATM)	XP_005271618.2:p.Tyr2334Ter
XM_005271562.3:c.7002del (ATM)	XP_005271619.2:p.Tyr2334Ter
XM_006718843.2:c.7002del (ATM)	XP_006718906.1:p.Tyr2334Ter
XM_006718845.1:c.2958del (ATM)	XP_006718908.1:p.Tyr986Ter
XM_011542840.1:c.7002del (ATM)	XP_011541142.1:p.Tyr2334Ter
XM_011542841.1:c.7002del (ATM)	XP_011541143.1:p.Tyr2334Ter
XM_011542842.1:c.6837del (ATM)	XP_011541144.1:p.Tyr2279Ter
XM_011542843.1:c.7002del (ATM)	XP_011541145.1:p.Tyr2334Ter
XM_011542844.1:c.5958del (ATM)	XP_011541146.1:p.Tyr1986Ter
XM_011542845.1:c.5694del (ATM)	XP_011541147.1:p.Tyr1898Ter
XM_011542847.1:c.2073del (ATM)	XP_011541149.1:p.Tyr691Ter
NM_001330368.1:c.641-18600del (C11orf65)	NP_001317297.1:n.641-18600del
NM_001351110.1:c.*38+7549del (C11orf65)	NP_001338039.1:n.*38+7549del
NM_001351834.1:c.7002del (ATM)	NP_001338763.1:p.Tyr2334Ter
XM_005271562.5:c.7002del (ATM)	XP_005271619.2:p.Tyr2334Ter
XM_006718843.4:c.7002del (ATM)	XP_006718906.1:p.Tyr2334Ter
XM_006718845.2:c.2958del (ATM)	XP_006718908.1:p.Tyr986Ter
XM_011542840.3:c.7002del (ATM)	XP_011541142.1:p.Tyr2334Ter
XM_011542842.3:c.6837del (ATM)	XP_011541144.1:p.Tyr2279Ter
XM_011542843.2:c.7002del (ATM)	XP_011541145.1:p.Tyr2334Ter
XM_011542844.3:c.5958del (ATM)	XP_011541146.1:p.Tyr1986Ter
XM_011542845.2:c.5694del (ATM)	XP_011541147.1:p.Tyr1898Ter
XM_017017789.2:c.7002del (ATM)	XP_016873278.1:p.Tyr2334Ter
XM_017017790.2:c.7002del (ATM)	XP_016873279.1:p.Tyr2334Ter
NM_001330368.2:c.641-18600del (C11orf65)	NP_001317297.1:n.641-18600del
NM_001351110.2:c.*38+7549del (C11orf65)	NP_001338039.1:n.*38+7549del
NM_001351834.2:c.7002del (ATM)	NP_001338763.1:p.Tyr2334Ter
NM_000051.4:c.7002del (ATM) MANE Select	NP_000042.3:p.Tyr2334Ter