Canonical Allele Identifier: CA1998799848

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108302922C= , CM000673.2:g.108302922C=	GRCh38
NC_000011.9:g.108173649C= , CM000673.1:g.108173649C=	GRCh37
NC_000011.8:g.107678859C=	NCBI36
NG_009830.1:g.85091C= , LRG_135:g.85091C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5389C=	ENSP00000388058.2:p.Pro1797=
ENST00000713593.1:c.*4860C=	ENSP00000518889.1:n.*4860C=
ENST00000278616.9:c.5389C=	ENSP00000278616.4:p.Pro1797=
ENST00000683174.1:n.6873C=
ENST00000683524.1:n.613C=
ENST00000684152.1:n.1103C=
ENST00000527805.6:c.*453C=	ENSP00000435747.2:n.*453C=
ENST00000675595.1:c.*453C=	ENSP00000502563.1:n.*453C=
ENST00000675843.1:c.5389C= MANE Select	ENSP00000501606.1:p.Pro1797=
ENST00000278616.8:c.5389C=	ENSP00000278616.4:p.Pro1797=
ENST00000452508.6:c.5389C=	ENSP00000388058.2:p.Pro1797=
ENST00000524792.5:n.1604C=
ENST00000533690.5:n.793C=
ENST00000534625.1:n.618C=
NM_000051.3:c.5389C= , LRG_135t1:c.5389C=	NP_000042.3:p.Pro1797=
XM_005271561.3:c.5389C=	XP_005271618.2:p.Pro1797=
XM_005271562.3:c.5389C=	XP_005271619.2:p.Pro1797=
XM_006718843.2:c.5389C=	XP_006718906.1:p.Pro1797=
XM_006718845.1:c.1345C=	XP_006718908.1:p.Pro449=
XM_011542840.1:c.5389C=	XP_011541142.1:p.Pro1797=
XM_011542841.1:c.5389C=	XP_011541143.1:p.Pro1797=
XM_011542842.1:c.5224C=	XP_011541144.1:p.Pro1742=
XM_011542843.1:c.5389C=	XP_011541145.1:p.Pro1797=
XM_011542844.1:c.4345C=	XP_011541146.1:p.Pro1449=
XM_011542845.1:c.4081C=	XP_011541147.1:p.Pro1361=
XM_011542846.1:c.*47C=	XP_011541148.1:n.*47C=
XM_011542847.1:c.460C=	XP_011541149.1:p.Pro154=
NM_001351834.1:c.5389C=	NP_001338763.1:p.Pro1797=
XM_005271562.5:c.5389C=	XP_005271619.2:p.Pro1797=
XM_006718843.4:c.5389C=	XP_006718906.1:p.Pro1797=
XM_006718845.2:c.1345C=	XP_006718908.1:p.Pro449=
XM_011542840.3:c.5389C=	XP_011541142.1:p.Pro1797=
XM_011542842.3:c.5224C=	XP_011541144.1:p.Pro1742=
XM_011542843.2:c.5389C=	XP_011541145.1:p.Pro1797=
XM_011542844.3:c.4345C=	XP_011541146.1:p.Pro1449=
XM_011542845.2:c.4081C=	XP_011541147.1:p.Pro1361=
XM_017017789.2:c.5389C=	XP_016873278.1:p.Pro1797=
XM_017017790.2:c.5389C=	XP_016873279.1:p.Pro1797=
XM_017017791.1:c.5389C=	XP_016873280.1:p.Pro1797=
XM_017017792.2:c.*70C=	XP_016873281.1:n.*70C=
XR_002957150.1:n.5989C=
NM_001351834.2:c.5389C=	NP_001338763.1:p.Pro1797=
NM_000051.4:c.5389C= MANE Select	NP_000042.3:p.Pro1797=