Canonical Allele Identifier: CA1998800873

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108315884G= , CM000673.2:g.108315884G=	GRCh38
NC_000011.9:g.108186611G= , CM000673.1:g.108186611G=	GRCh37
NC_000011.8:g.107691821G=	NCBI36
NG_009830.1:g.98053G= , LRG_135:g.98053G=
NG_054724.1:g.158949C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6068G= (ATM)	ENSP00000388058.2:p.Gly2023=
ENST00000713593.1:c.*5539G= (ATM)	ENSP00000518889.1:n.*5539G=
ENST00000278616.9:c.6068G= (ATM)	ENSP00000278616.4:p.Gly2023=
ENST00000525056.2:n.487G= (ATM)
ENST00000682286.1:n.825G= (ATM)
ENST00000682302.1:n.486G= (ATM)
ENST00000683174.1:n.7552G= (ATM)
ENST00000683524.1:n.1292G= (ATM)
ENST00000684152.1:n.1782G= (ATM)
ENST00000527805.6:c.*1132G= (ATM)	ENSP00000435747.2:n.*1132G=
ENST00000675595.1:c.*1132G= (ATM)	ENSP00000502563.1:n.*1132G=
ENST00000675843.1:c.6068G= (ATM) MANE Select	ENSP00000501606.1:p.Gly2023=
ENST00000278616.8:c.6068G= (ATM)	ENSP00000278616.4:p.Gly2023=
ENST00000452508.6:c.6068G= (ATM)	ENSP00000388058.2:p.Gly2023=
ENST00000524792.5:n.2283G= (ATM)
ENST00000525729.5:c.641-6813C= (C11orf65)	ENSP00000433395.1:n.641-6813C=
ENST00000529588.5:c.492G= (ATM)
ENST00000532765.1:n.385G= (ATM)
ENST00000533690.5:n.1472G= (ATM)
NM_000051.3:c.6068G= , LRG_135t1:c.6068G= (ATM)	NP_000042.3:p.Gly2023=
XM_005271561.3:c.6068G= (ATM)	XP_005271618.2:p.Gly2023=
XM_005271562.3:c.6068G= (ATM)	XP_005271619.2:p.Gly2023=
XM_006718843.2:c.6068G= (ATM)	XP_006718906.1:p.Gly2023=
XM_006718845.1:c.2024G= (ATM)	XP_006718908.1:p.Gly675=
XM_011542840.1:c.6068G= (ATM)	XP_011541142.1:p.Gly2023=
XM_011542841.1:c.6068G= (ATM)	XP_011541143.1:p.Gly2023=
XM_011542842.1:c.5903G= (ATM)	XP_011541144.1:p.Gly1968=
XM_011542843.1:c.6068G= (ATM)	XP_011541145.1:p.Gly2023=
XM_011542844.1:c.5024G= (ATM)	XP_011541146.1:p.Gly1675=
XM_011542845.1:c.4760G= (ATM)	XP_011541147.1:p.Gly1587=
XM_011542847.1:c.1139G= (ATM)	XP_011541149.1:p.Gly380=
NM_001330368.1:c.641-6813C= (C11orf65)	NP_001317297.1:n.641-6813C=
NM_001351110.1:c.*39-6813C= (C11orf65)	NP_001338039.1:n.*39-6813C=
NM_001351834.1:c.6068G= (ATM)	NP_001338763.1:p.Gly2023=
XM_005271562.5:c.6068G= (ATM)	XP_005271619.2:p.Gly2023=
XM_006718843.4:c.6068G= (ATM)	XP_006718906.1:p.Gly2023=
XM_006718845.2:c.2024G= (ATM)	XP_006718908.1:p.Gly675=
XM_011542840.3:c.6068G= (ATM)	XP_011541142.1:p.Gly2023=
XM_011542842.3:c.5903G= (ATM)	XP_011541144.1:p.Gly1968=
XM_011542843.2:c.6068G= (ATM)	XP_011541145.1:p.Gly2023=
XM_011542844.3:c.5024G= (ATM)	XP_011541146.1:p.Gly1675=
XM_011542845.2:c.4760G= (ATM)	XP_011541147.1:p.Gly1587=
XM_017017789.2:c.6068G= (ATM)	XP_016873278.1:p.Gly2023=
XM_017017790.2:c.6068G= (ATM)	XP_016873279.1:p.Gly2023=
XM_017017791.1:c.6068G= (ATM)	XP_016873280.1:p.Gly2023=
NM_001330368.2:c.641-6813C= (C11orf65)	NP_001317297.1:n.641-6813C=
NM_001351110.2:c.*39-6813C= (C11orf65)	NP_001338039.1:n.*39-6813C=
NM_001351834.2:c.6068G= (ATM)	NP_001338763.1:p.Gly2023=
NM_000051.4:c.6068G= (ATM) MANE Select	NP_000042.3:p.Gly2023=