Canonical Allele Identifier: CA1998790251

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108282731A= , CM000673.2:g.108282731A=	GRCh38
NC_000011.9:g.108153458A= , CM000673.1:g.108153458A=	GRCh37
NC_000011.8:g.107658668A=	NCBI36
NG_009830.1:g.64900A= , LRG_135:g.64900A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.3598A=	ENSP00000388058.2:p.Thr1200=
ENST00000713593.1:c.*3069A=	ENSP00000518889.1:n.*3069A=
ENST00000278616.9:c.3598A=	ENSP00000278616.4:p.Thr1200=
ENST00000683174.1:n.3748A=
ENST00000527805.6:c.3598A=	ENSP00000435747.2:p.Thr1200=
ENST00000675595.1:c.3433A=	ENSP00000502563.1:p.Thr1145=
ENST00000675843.1:c.3598A= MANE Select	ENSP00000501606.1:p.Thr1200=
ENST00000278616.8:c.3598A=	ENSP00000278616.4:p.Thr1200=
ENST00000452508.6:c.3598A=	ENSP00000388058.2:p.Thr1200=
ENST00000527805.5:c.3598A=	ENSP00000435747.1:p.Thr1200=
NM_000051.3:c.3598A= , LRG_135t1:c.3598A=	NP_000042.3:p.Thr1200=
XM_005271561.3:c.3598A=	XP_005271618.2:p.Thr1200=
XM_005271562.3:c.3598A=	XP_005271619.2:p.Thr1200=
XM_006718843.2:c.3598A=	XP_006718906.1:p.Thr1200=
XM_011542840.1:c.3598A=	XP_011541142.1:p.Thr1200=
XM_011542841.1:c.3598A=	XP_011541143.1:p.Thr1200=
XM_011542842.1:c.3433A=	XP_011541144.1:p.Thr1145=
XM_011542843.1:c.3598A=	XP_011541145.1:p.Thr1200=
XM_011542844.1:c.2554A=	XP_011541146.1:p.Thr852=
XM_011542845.1:c.2290A=	XP_011541147.1:p.Thr764=
XM_011542846.1:c.3598A=	XP_011541148.1:p.Thr1200=
NM_001351834.1:c.3598A=	NP_001338763.1:p.Thr1200=
XM_005271562.5:c.3598A=	XP_005271619.2:p.Thr1200=
XM_006718843.4:c.3598A=	XP_006718906.1:p.Thr1200=
XM_011542840.3:c.3598A=	XP_011541142.1:p.Thr1200=
XM_011542842.3:c.3433A=	XP_011541144.1:p.Thr1145=
XM_011542843.2:c.3598A=	XP_011541145.1:p.Thr1200=
XM_011542844.3:c.2554A=	XP_011541146.1:p.Thr852=
XM_011542845.2:c.2290A=	XP_011541147.1:p.Thr764=
XM_017017789.2:c.3598A=	XP_016873278.1:p.Thr1200=
XM_017017790.2:c.3598A=	XP_016873279.1:p.Thr1200=
XM_017017791.1:c.3598A=	XP_016873280.1:p.Thr1200=
XM_017017792.2:c.3598A=	XP_016873281.1:p.Thr1200=
XR_002957150.1:n.4331A=
NM_001351834.2:c.3598A=	NP_001338763.1:p.Thr1200=
NM_000051.4:c.3598A= MANE Select	NP_000042.3:p.Thr1200=