Canonical Allele Identifier: CA1998811389

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108332878C= , CM000673.2:g.108332878C=	GRCh38
NC_000011.9:g.108203605C= , CM000673.1:g.108203605C=	GRCh37
NC_000011.8:g.107708815C=	NCBI36
NG_009830.1:g.115047C= , LRG_135:g.115047C=
NG_054724.1:g.141955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7905C= (ATM)	ENSP00000388058.2:p.Ala2635=
ENST00000713593.1:c.*7376C= (ATM)	ENSP00000518889.1:n.*7376C=
ENST00000278616.9:c.7905C= (ATM)	ENSP00000278616.4:p.Ala2635=
ENST00000525056.2:n.2324C= (ATM)
ENST00000525537.3:n.1586C= (ATM)
ENST00000638786.2:n.625+841C= (ATM)
ENST00000682286.1:n.2662C= (ATM)
ENST00000682302.1:n.2323C= (ATM)
ENST00000683174.1:n.9389C= (ATM)
ENST00000683524.1:n.3129C= (ATM)
ENST00000684152.1:n.3344-1008C= (ATM)
ENST00000684180.1:n.379C= (ATM)
ENST00000684447.1:n.3413C= (ATM)
ENST00000527805.6:c.*2969C= (ATM)	ENSP00000435747.2:n.*2969C=
ENST00000675595.1:c.*3040C= (ATM)	ENSP00000502563.1:n.*3040C=
ENST00000675843.1:c.7905C= (ATM) MANE Select	ENSP00000501606.1:p.Ala2635=
ENST00000278616.8:c.7905C= (ATM)	ENSP00000278616.4:p.Ala2635=
ENST00000452508.6:c.7905C= (ATM)	ENSP00000388058.2:p.Ala2635=
ENST00000524755.5:c.300-1311G= (C11orf65)
ENST00000524792.5:n.4120C= (ATM)
ENST00000525056.1:n.102C= (ATM)
ENST00000525729.5:c.641-23807G= (C11orf65)	ENSP00000433395.1:n.641-23807G=
ENST00000527531.5:c.*1270-1311G= (C11orf65)	ENSP00000431706.1:n.*1270-1311G=
ENST00000533690.5:n.3309C= (ATM)
ENST00000533979.5:n.117C= (ATM)
ENST00000615746.4:c.*1270-1311G= (C11orf65)	ENSP00000483537.1:n.*1270-1311G=
NM_000051.3:c.7905C= , LRG_135t1:c.7905C= (ATM)	NP_000042.3:p.Ala2635=
XM_005271414.3:c.*39-1311G= (C11orf65)	XP_005271471.1:n.*39-1311G=
XM_005271415.3:c.805-1311G= (C11orf65)	XP_005271472.1:n.805-1311G=
XM_005271561.3:c.7905C= (ATM)	XP_005271618.2:p.Ala2635=
XM_005271562.3:c.7905C= (ATM)	XP_005271619.2:p.Ala2635=
XM_006718843.2:c.7905C= (ATM)	XP_006718906.1:p.Ala2635=
XM_006718845.1:c.3861C= (ATM)	XP_006718908.1:p.Ala1287=
XM_011542840.1:c.7905C= (ATM)	XP_011541142.1:p.Ala2635=
XM_011542841.1:c.7905C= (ATM)	XP_011541143.1:p.Ala2635=
XM_011542842.1:c.7740C= (ATM)	XP_011541144.1:p.Ala2580=
XM_011542843.1:c.7905C= (ATM)	XP_011541145.1:p.Ala2635=
XM_011542844.1:c.6861C= (ATM)	XP_011541146.1:p.Ala2287=
XM_011542845.1:c.6597C= (ATM)	XP_011541147.1:p.Ala2199=
XM_011542847.1:c.2976C= (ATM)	XP_011541149.1:p.Ala992=
NM_001330368.1:c.641-23807G= (C11orf65)	NP_001317297.1:n.641-23807G=
NM_001351110.1:c.*38+2342G= (C11orf65)	NP_001338039.1:n.*38+2342G=
NM_001351834.1:c.7905C= (ATM)	NP_001338763.1:p.Ala2635=
NR_147053.2:n.2375-1311G= (C11orf65)
XM_005271414.4:c.*39-1311G= (C11orf65)	XP_005271471.1:n.*39-1311G=
XM_005271415.4:c.805-1311G= (C11orf65)	XP_005271472.1:n.805-1311G=
XM_005271562.5:c.7905C= (ATM)	XP_005271619.2:p.Ala2635=
XM_006718843.4:c.7905C= (ATM)	XP_006718906.1:p.Ala2635=
XM_006718845.2:c.3861C= (ATM)	XP_006718908.1:p.Ala1287=
XM_011542840.3:c.7905C= (ATM)	XP_011541142.1:p.Ala2635=
XM_011542842.3:c.7740C= (ATM)	XP_011541144.1:p.Ala2580=
XM_011542843.2:c.7905C= (ATM)	XP_011541145.1:p.Ala2635=
XM_011542844.3:c.6861C= (ATM)	XP_011541146.1:p.Ala2287=
XM_011542845.2:c.6597C= (ATM)	XP_011541147.1:p.Ala2199=
XM_017017789.2:c.7905C= (ATM)	XP_016873278.1:p.Ala2635=
XM_017017790.2:c.7905C= (ATM)	XP_016873279.1:p.Ala2635=
NM_001330368.2:c.641-23807G= (C11orf65)	NP_001317297.1:n.641-23807G=
NM_001351110.2:c.*38+2342G= (C11orf65)	NP_001338039.1:n.*38+2342G=
NM_001351834.2:c.7905C= (ATM)	NP_001338763.1:p.Ala2635=
NM_000051.4:c.7905C= (ATM) MANE Select	NP_000042.3:p.Ala2635=
NR_147053.3:n.2373-1311G= (C11orf65)