Canonical Allele Identifier: CA1998811421

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108332925G= , CM000673.2:g.108332925G=	GRCh38
NC_000011.9:g.108203652G= , CM000673.1:g.108203652G=	GRCh37
NC_000011.8:g.107708862G=	NCBI36
NG_009830.1:g.115094G= , LRG_135:g.115094G=
NG_054724.1:g.141908C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7927+25G= (ATM)	ENSP00000388058.2:n.7927+25G=
ENST00000713593.1:c.*7398+25G= (ATM)	ENSP00000518889.1:n.*7398+25G=
ENST00000278616.9:c.7927+25G= (ATM)	ENSP00000278616.4:n.7927+25G=
ENST00000525056.2:n.2346+25G= (ATM)
ENST00000525537.3:n.1633G= (ATM)
ENST00000638786.2:n.625+888G= (ATM)
ENST00000682286.1:n.2684+25G= (ATM)
ENST00000682302.1:n.2345+25G= (ATM)
ENST00000683174.1:n.9411+25G= (ATM)
ENST00000683524.1:n.3151+25G= (ATM)
ENST00000684152.1:n.3344-961G= (ATM)
ENST00000684180.1:n.401+25G= (ATM)
ENST00000684447.1:n.3460G= (ATM)
ENST00000527805.6:c.*2991+25G= (ATM)	ENSP00000435747.2:n.*2991+25G=
ENST00000675595.1:c.*3062+25G= (ATM)	ENSP00000502563.1:n.*3062+25G=
ENST00000675843.1:c.7927+25G= (ATM) MANE Select	ENSP00000501606.1:n.7927+25G=
ENST00000278616.8:c.7927+25G= (ATM)	ENSP00000278616.4:n.7927+25G=
ENST00000452508.6:c.7927+25G= (ATM)	ENSP00000388058.2:n.7927+25G=
ENST00000524755.5:c.300-1358C= (C11orf65)
ENST00000524792.5:n.4142+25G= (ATM)
ENST00000525056.1:n.124+25G= (ATM)
ENST00000525729.5:c.641-23854C= (C11orf65)	ENSP00000433395.1:n.641-23854C=
ENST00000527531.5:c.*1270-1358C= (C11orf65)	ENSP00000431706.1:n.*1270-1358C=
ENST00000533690.5:n.3331+25G= (ATM)
ENST00000533979.5:n.139+25G= (ATM)
ENST00000615746.4:c.*1270-1358C= (C11orf65)	ENSP00000483537.1:n.*1270-1358C=
NM_000051.3:c.7927+25G= , LRG_135t1:c.7927+25G= (ATM)	NP_000042.3:n.7927+25G=
XM_005271414.3:c.*39-1358C= (C11orf65)	XP_005271471.1:n.*39-1358C=
XM_005271415.3:c.805-1358C= (C11orf65)	XP_005271472.1:n.805-1358C=
XM_005271561.3:c.7927+25G= (ATM)	XP_005271618.2:n.7927+25G=
XM_005271562.3:c.7927+25G= (ATM)	XP_005271619.2:n.7927+25G=
XM_006718843.2:c.7927+25G= (ATM)	XP_006718906.1:n.7927+25G=
XM_006718845.1:c.3883+25G= (ATM)	XP_006718908.1:n.3883+25G=
XM_011542840.1:c.7927+25G= (ATM)	XP_011541142.1:n.7927+25G=
XM_011542841.1:c.7927+25G= (ATM)	XP_011541143.1:n.7927+25G=
XM_011542842.1:c.7762+25G= (ATM)	XP_011541144.1:n.7762+25G=
XM_011542843.1:c.7927+25G= (ATM)	XP_011541145.1:n.7927+25G=
XM_011542844.1:c.6883+25G= (ATM)	XP_011541146.1:n.6883+25G=
XM_011542845.1:c.6619+25G= (ATM)	XP_011541147.1:n.6619+25G=
XM_011542847.1:c.2998+25G= (ATM)	XP_011541149.1:n.2998+25G=
NM_001330368.1:c.641-23854C= (C11orf65)	NP_001317297.1:n.641-23854C=
NM_001351110.1:c.*38+2295C= (C11orf65)	NP_001338039.1:n.*38+2295C=
NM_001351834.1:c.7927+25G= (ATM)	NP_001338763.1:n.7927+25G=
NR_147053.2:n.2375-1358C= (C11orf65)
XM_005271414.4:c.*39-1358C= (C11orf65)	XP_005271471.1:n.*39-1358C=
XM_005271415.4:c.805-1358C= (C11orf65)	XP_005271472.1:n.805-1358C=
XM_005271562.5:c.7927+25G= (ATM)	XP_005271619.2:n.7927+25G=
XM_006718843.4:c.7927+25G= (ATM)	XP_006718906.1:n.7927+25G=
XM_006718845.2:c.3883+25G= (ATM)	XP_006718908.1:n.3883+25G=
XM_011542840.3:c.7927+25G= (ATM)	XP_011541142.1:n.7927+25G=
XM_011542842.3:c.7762+25G= (ATM)	XP_011541144.1:n.7762+25G=
XM_011542843.2:c.7927+25G= (ATM)	XP_011541145.1:n.7927+25G=
XM_011542844.3:c.6883+25G= (ATM)	XP_011541146.1:n.6883+25G=
XM_011542845.2:c.6619+25G= (ATM)	XP_011541147.1:n.6619+25G=
XM_017017789.2:c.7927+25G= (ATM)	XP_016873278.1:n.7927+25G=
XM_017017790.2:c.7927+25G= (ATM)	XP_016873279.1:n.7927+25G=
NM_001330368.2:c.641-23854C= (C11orf65)	NP_001317297.1:n.641-23854C=
NM_001351110.2:c.*38+2295C= (C11orf65)	NP_001338039.1:n.*38+2295C=
NM_001351834.2:c.7927+25G= (ATM)	NP_001338763.1:n.7927+25G=
NM_000051.4:c.7927+25G= (ATM) MANE Select	NP_000042.3:n.7927+25G=
NR_147053.3:n.2373-1358C= (C11orf65)