Canonical Allele Identifier: CA1998796424

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108310161_108310164delinsCCTT , CM000673.2:g.108310161_108310164delinsCCTT	GRCh38
NC_000011.9:g.108180888_108180891delinsCCTT , CM000673.1:g.108180888_108180891delinsCCTT	GRCh37
NC_000011.8:g.107686098_107686101delinsCCTT	NCBI36
NG_009830.1:g.92330_92333delinsCCTT , LRG_135:g.92330_92333delinsCCTT
NG_054724.1:g.164669_164672delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5764_5767delinsCCTT (ATM)	ENSP00000388058.2:p.Pro1922=
ENST00000713593.1:c.*5235_*5238delinsCCTT (ATM)	ENSP00000518889.1:n.*5235_*5238delinsCCTT
ENST00000278616.9:c.5764_5767delinsCCTT (ATM)	ENSP00000278616.4:p.Pro1922=
ENST00000525056.2:n.183_186delinsCCTT (ATM)
ENST00000682286.1:n.521_524delinsCCTT (ATM)
ENST00000682302.1:n.182_185delinsCCTT (ATM)
ENST00000683174.1:n.7248_7251delinsCCTT (ATM)
ENST00000683524.1:n.988_991delinsCCTT (ATM)
ENST00000684152.1:n.1478_1481delinsCCTT (ATM)
ENST00000527805.6:c.*828_*831delinsCCTT (ATM)	ENSP00000435747.2:n.*828_*831delinsCCTT
ENST00000675595.1:c.*828_*831delinsCCTT (ATM)	ENSP00000502563.1:n.*828_*831delinsCCTT
ENST00000675843.1:c.5764_5767delinsCCTT (ATM) MANE Select	ENSP00000501606.1:p.Pro1922=
ENST00000278616.8:c.5764_5767delinsCCTT (ATM)	ENSP00000278616.4:p.Pro1922=
ENST00000452508.6:c.5764_5767delinsCCTT (ATM)	ENSP00000388058.2:p.Pro1922=
ENST00000524792.5:n.1979_1982delinsCCTT (ATM)
ENST00000525729.5:c.641-1093_641-1090delinsAAGG (C11orf65)	ENSP00000433395.1:n.641-1093_641-1090delinsAAGG
ENST00000529588.5:c.188_191delinsCCTT (ATM)
ENST00000532765.1:n.81_84delinsCCTT (ATM)
ENST00000533690.5:n.1168_1171delinsCCTT (ATM)
NM_000051.3:c.5764_5767delinsCCTT , LRG_135t1:c.5764_5767delinsCCTT (ATM)	NP_000042.3:p.Pro1922=
XM_005271561.3:c.5764_5767delinsCCTT (ATM)	XP_005271618.2:p.Pro1922=
XM_005271562.3:c.5764_5767delinsCCTT (ATM)	XP_005271619.2:p.Pro1922=
XM_006718843.2:c.5764_5767delinsCCTT (ATM)	XP_006718906.1:p.Pro1922=
XM_006718845.1:c.1720_1723delinsCCTT (ATM)	XP_006718908.1:p.Pro574=
XM_011542840.1:c.5764_5767delinsCCTT (ATM)	XP_011541142.1:p.Pro1922=
XM_011542841.1:c.5764_5767delinsCCTT (ATM)	XP_011541143.1:p.Pro1922=
XM_011542842.1:c.5599_5602delinsCCTT (ATM)	XP_011541144.1:p.Pro1867=
XM_011542843.1:c.5764_5767delinsCCTT (ATM)	XP_011541145.1:p.Pro1922=
XM_011542844.1:c.4720_4723delinsCCTT (ATM)	XP_011541146.1:p.Pro1574=
XM_011542845.1:c.4456_4459delinsCCTT (ATM)	XP_011541147.1:p.Pro1486=
XM_011542847.1:c.835_838delinsCCTT (ATM)	XP_011541149.1:p.Pro279=
NM_001330368.1:c.641-1093_641-1090delinsAAGG (C11orf65)	NP_001317297.1:n.641-1093_641-1090delinsAAGG
NM_001351110.1:c.*39-1093_*39-1090delinsAAGG (C11orf65)	NP_001338039.1:n.*39-1093_*39-1090delinsAAGG
NM_001351834.1:c.5764_5767delinsCCTT (ATM)	NP_001338763.1:p.Pro1922=
XM_005271562.5:c.5764_5767delinsCCTT (ATM)	XP_005271619.2:p.Pro1922=
XM_006718843.4:c.5764_5767delinsCCTT (ATM)	XP_006718906.1:p.Pro1922=
XM_006718845.2:c.1720_1723delinsCCTT (ATM)	XP_006718908.1:p.Pro574=
XM_011542840.3:c.5764_5767delinsCCTT (ATM)	XP_011541142.1:p.Pro1922=
XM_011542842.3:c.5599_5602delinsCCTT (ATM)	XP_011541144.1:p.Pro1867=
XM_011542843.2:c.5764_5767delinsCCTT (ATM)	XP_011541145.1:p.Pro1922=
XM_011542844.3:c.4720_4723delinsCCTT (ATM)	XP_011541146.1:p.Pro1574=
XM_011542845.2:c.4456_4459delinsCCTT (ATM)	XP_011541147.1:p.Pro1486=
XM_017017789.2:c.5764_5767delinsCCTT (ATM)	XP_016873278.1:p.Pro1922=
XM_017017790.2:c.5764_5767delinsCCTT (ATM)	XP_016873279.1:p.Pro1922=
XM_017017791.1:c.5764_5767delinsCCTT (ATM)	XP_016873280.1:p.Pro1922=
XR_002957150.1:n.6364_6367delinsCCTT (ATM)
NM_001330368.2:c.641-1093_641-1090delinsAAGG (C11orf65)	NP_001317297.1:n.641-1093_641-1090delinsAAGG
NM_001351110.2:c.*39-1093_*39-1090delinsAAGG (C11orf65)	NP_001338039.1:n.*39-1093_*39-1090delinsAAGG
NM_001351834.2:c.5764_5767delinsCCTT (ATM)	NP_001338763.1:p.Pro1922=
NM_000051.4:c.5764_5767delinsCCTT (ATM) MANE Select	NP_000042.3:p.Pro1922=