Canonical Allele Identifier: CA1998772436

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253946T= , CM000673.2:g.108253946T=	GRCh38
NC_000011.9:g.108124673T= , CM000673.1:g.108124673T=	GRCh37
NC_000011.8:g.107629883T=	NCBI36
NG_009830.1:g.36115T= , LRG_135:g.36115T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2031T=	ENSP00000388058.2:p.Ser677=
ENST00000713593.1:c.*1502T=	ENSP00000518889.1:n.*1502T=
ENST00000278616.9:c.2031T=	ENSP00000278616.4:p.Ser677=
ENST00000682516.1:n.2165T=
ENST00000683174.1:n.2181T=
ENST00000683605.1:n.1526T=
ENST00000684037.1:c.*966T=	ENSP00000508245.1:n.*966T=
ENST00000684061.1:n.2165T=
ENST00000527805.6:c.2031T=	ENSP00000435747.2:p.Ser677=
ENST00000675595.1:c.1866T=	ENSP00000502563.1:p.Ser622=
ENST00000675843.1:c.2031T= MANE Select	ENSP00000501606.1:p.Ser677=
ENST00000278616.8:c.2031T=	ENSP00000278616.4:p.Ser677=
ENST00000452508.6:c.2031T=	ENSP00000388058.2:p.Ser677=
ENST00000525012.5:n.208T=
ENST00000527805.5:c.2031T=	ENSP00000435747.1:p.Ser677=
ENST00000533526.1:n.184T=
NM_000051.3:c.2031T= , LRG_135t1:c.2031T=	NP_000042.3:p.Ser677=
XM_005271561.3:c.2031T=	XP_005271618.2:p.Ser677=
XM_005271562.3:c.2031T=	XP_005271619.2:p.Ser677=
XM_006718843.2:c.2031T=	XP_006718906.1:p.Ser677=
XM_011542840.1:c.2031T=	XP_011541142.1:p.Ser677=
XM_011542841.1:c.2031T=	XP_011541143.1:p.Ser677=
XM_011542842.1:c.1866T=	XP_011541144.1:p.Ser622=
XM_011542843.1:c.2031T=	XP_011541145.1:p.Ser677=
XM_011542844.1:c.987T=	XP_011541146.1:p.Ser329=
XM_011542845.1:c.723T=	XP_011541147.1:p.Ser241=
XM_011542846.1:c.2031T=	XP_011541148.1:p.Ser677=
NM_001351834.1:c.2031T=	NP_001338763.1:p.Ser677=
XM_005271562.5:c.2031T=	XP_005271619.2:p.Ser677=
XM_006718843.4:c.2031T=	XP_006718906.1:p.Ser677=
XM_011542840.3:c.2031T=	XP_011541142.1:p.Ser677=
XM_011542842.3:c.1866T=	XP_011541144.1:p.Ser622=
XM_011542843.2:c.2031T=	XP_011541145.1:p.Ser677=
XM_011542844.3:c.987T=	XP_011541146.1:p.Ser329=
XM_011542845.2:c.723T=	XP_011541147.1:p.Ser241=
XM_017017789.2:c.2031T=	XP_016873278.1:p.Ser677=
XM_017017790.2:c.2031T=	XP_016873279.1:p.Ser677=
XM_017017791.1:c.2031T=	XP_016873280.1:p.Ser677=
XM_017017792.2:c.2031T=	XP_016873281.1:p.Ser677=
XR_002957150.1:n.2764T=
NM_001351834.2:c.2031T=	NP_001338763.1:p.Ser677=
NM_000051.4:c.2031T= MANE Select	NP_000042.3:p.Ser677=