Canonical Allele Identifier: CA1998805478

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108319947_108319948delinsCT , CM000673.2:g.108319947_108319948delinsCT	GRCh38
NC_000011.9:g.108190674_108190675delinsCT , CM000673.1:g.108190674_108190675delinsCT	GRCh37
NC_000011.8:g.107695884_107695885delinsCT	NCBI36
NG_009830.1:g.102116_102117delinsCT , LRG_135:g.102116_102117delinsCT
NG_054724.1:g.154885_154886delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6348-7_6348-6delinsCT (ATM)	ENSP00000388058.2:n.6348-7_6348-6delinsCT
ENST00000713593.1:c.*5819-7_*5819-6delinsCT (ATM)	ENSP00000518889.1:n.*5819-7_*5819-6delinsCT
ENST00000278616.9:c.6348-7_6348-6delinsCT (ATM)	ENSP00000278616.4:n.6348-7_6348-6delinsCT
ENST00000525056.2:n.767-7_767-6delinsCT (ATM)
ENST00000682286.1:n.1105-7_1105-6delinsCT (ATM)
ENST00000682302.1:n.766-7_766-6delinsCT (ATM)
ENST00000683174.1:n.7832-7_7832-6delinsCT (ATM)
ENST00000683524.1:n.1572-7_1572-6delinsCT (ATM)
ENST00000684152.1:n.2062-7_2062-6delinsCT (ATM)
ENST00000527805.6:c.*1412-7_*1412-6delinsCT (ATM)	ENSP00000435747.2:n.*1412-7_*1412-6delinsCT
ENST00000675595.1:c.*1412-7_*1412-6delinsCT (ATM)	ENSP00000502563.1:n.*1412-7_*1412-6delinsCT
ENST00000675843.1:c.6348-7_6348-6delinsCT (ATM) MANE Select	ENSP00000501606.1:n.6348-7_6348-6delinsCT
ENST00000278616.8:c.6348-7_6348-6delinsCT (ATM)	ENSP00000278616.4:n.6348-7_6348-6delinsCT
ENST00000452508.6:c.6348-7_6348-6delinsCT (ATM)	ENSP00000388058.2:n.6348-7_6348-6delinsCT
ENST00000524792.5:n.2563-7_2563-6delinsCT (ATM)
ENST00000525729.5:c.641-10877_641-10876delinsAG (C11orf65)	ENSP00000433395.1:n.641-10877_641-10876delinsAG
ENST00000533690.5:n.1752-7_1752-6delinsCT (ATM)
NM_000051.3:c.6348-7_6348-6delinsCT , LRG_135t1:c.6348-7_6348-6delinsCT (ATM)	NP_000042.3:n.6348-7_6348-6delinsCT
XM_005271561.3:c.6348-7_6348-6delinsCT (ATM)	XP_005271618.2:n.6348-7_6348-6delinsCT
XM_005271562.3:c.6348-7_6348-6delinsCT (ATM)	XP_005271619.2:n.6348-7_6348-6delinsCT
XM_006718843.2:c.6348-7_6348-6delinsCT (ATM)	XP_006718906.1:n.6348-7_6348-6delinsCT
XM_006718845.1:c.2304-7_2304-6delinsCT (ATM)	XP_006718908.1:n.2304-7_2304-6delinsCT
XM_011542840.1:c.6348-7_6348-6delinsCT (ATM)	XP_011541142.1:n.6348-7_6348-6delinsCT
XM_011542841.1:c.6348-7_6348-6delinsCT (ATM)	XP_011541143.1:n.6348-7_6348-6delinsCT
XM_011542842.1:c.6183-7_6183-6delinsCT (ATM)	XP_011541144.1:n.6183-7_6183-6delinsCT
XM_011542843.1:c.6348-7_6348-6delinsCT (ATM)	XP_011541145.1:n.6348-7_6348-6delinsCT
XM_011542844.1:c.5304-7_5304-6delinsCT (ATM)	XP_011541146.1:n.5304-7_5304-6delinsCT
XM_011542845.1:c.5040-7_5040-6delinsCT (ATM)	XP_011541147.1:n.5040-7_5040-6delinsCT
XM_011542847.1:c.1419-7_1419-6delinsCT (ATM)	XP_011541149.1:n.1419-7_1419-6delinsCT
NM_001330368.1:c.641-10877_641-10876delinsAG (C11orf65)	NP_001317297.1:n.641-10877_641-10876delinsAG
NM_001351110.1:c.*39-10877_*39-10876delinsAG (C11orf65)	NP_001338039.1:n.*39-10877_*39-10876delinsAG
NM_001351834.1:c.6348-7_6348-6delinsCT (ATM)	NP_001338763.1:n.6348-7_6348-6delinsCT
XM_005271562.5:c.6348-7_6348-6delinsCT (ATM)	XP_005271619.2:n.6348-7_6348-6delinsCT
XM_006718843.4:c.6348-7_6348-6delinsCT (ATM)	XP_006718906.1:n.6348-7_6348-6delinsCT
XM_006718845.2:c.2304-7_2304-6delinsCT (ATM)	XP_006718908.1:n.2304-7_2304-6delinsCT
XM_011542840.3:c.6348-7_6348-6delinsCT (ATM)	XP_011541142.1:n.6348-7_6348-6delinsCT
XM_011542842.3:c.6183-7_6183-6delinsCT (ATM)	XP_011541144.1:n.6183-7_6183-6delinsCT
XM_011542843.2:c.6348-7_6348-6delinsCT (ATM)	XP_011541145.1:n.6348-7_6348-6delinsCT
XM_011542844.3:c.5304-7_5304-6delinsCT (ATM)	XP_011541146.1:n.5304-7_5304-6delinsCT
XM_011542845.2:c.5040-7_5040-6delinsCT (ATM)	XP_011541147.1:n.5040-7_5040-6delinsCT
XM_017017789.2:c.6348-7_6348-6delinsCT (ATM)	XP_016873278.1:n.6348-7_6348-6delinsCT
XM_017017790.2:c.6348-7_6348-6delinsCT (ATM)	XP_016873279.1:n.6348-7_6348-6delinsCT
XM_017017791.1:c.6348-7_6348-6delinsCT (ATM)	XP_016873280.1:n.6348-7_6348-6delinsCT
NM_001330368.2:c.641-10877_641-10876delinsAG (C11orf65)	NP_001317297.1:n.641-10877_641-10876delinsAG
NM_001351110.2:c.*39-10877_*39-10876delinsAG (C11orf65)	NP_001338039.1:n.*39-10877_*39-10876delinsAG
NM_001351834.2:c.6348-7_6348-6delinsCT (ATM)	NP_001338763.1:n.6348-7_6348-6delinsCT
NM_000051.4:c.6348-7_6348-6delinsCT (ATM) MANE Select	NP_000042.3:n.6348-7_6348-6delinsCT