Canonical Allele Identifier: CA1998809359

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327585G= , CM000673.2:g.108327585G=	GRCh38
NC_000011.9:g.108198312G= , CM000673.1:g.108198312G=	GRCh37
NC_000011.8:g.107703522G=	NCBI36
NG_009830.1:g.109754G= , LRG_135:g.109754G=
NG_054724.1:g.147248C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6976-60G= (ATM)	ENSP00000388058.2:n.6976-60G=
ENST00000713593.1:c.*6447-60G= (ATM)	ENSP00000518889.1:n.*6447-60G=
ENST00000278616.9:c.6976-60G= (ATM)	ENSP00000278616.4:n.6976-60G=
ENST00000525056.2:n.1395-60G= (ATM)
ENST00000682286.1:n.1733-60G= (ATM)
ENST00000682302.1:n.1394-60G= (ATM)
ENST00000683174.1:n.8460-60G= (ATM)
ENST00000683524.1:n.2200-60G= (ATM)
ENST00000684152.1:n.2690-60G= (ATM)
ENST00000684447.1:n.1379G= (ATM)
ENST00000527805.6:c.*2040-60G= (ATM)	ENSP00000435747.2:n.*2040-60G=
ENST00000675595.1:c.*2111-60G= (ATM)	ENSP00000502563.1:n.*2111-60G=
ENST00000675843.1:c.6976-60G= (ATM) MANE Select	ENSP00000501606.1:n.6976-60G=
ENST00000278616.8:c.6976-60G= (ATM)	ENSP00000278616.4:n.6976-60G=
ENST00000452508.6:c.6976-60G= (ATM)	ENSP00000388058.2:n.6976-60G=
ENST00000524792.5:n.3191-60G= (ATM)
ENST00000525537.2:n.192G= (ATM)
ENST00000525729.5:c.641-18514C= (C11orf65)	ENSP00000433395.1:n.641-18514C=
ENST00000533690.5:n.2380-60G= (ATM)
NM_000051.3:c.6976-60G= , LRG_135t1:c.6976-60G= (ATM)	NP_000042.3:n.6976-60G=
XM_005271561.3:c.6976-60G= (ATM)	XP_005271618.2:n.6976-60G=
XM_005271562.3:c.6976-60G= (ATM)	XP_005271619.2:n.6976-60G=
XM_006718843.2:c.6976-60G= (ATM)	XP_006718906.1:n.6976-60G=
XM_006718845.1:c.2932-60G= (ATM)	XP_006718908.1:n.2932-60G=
XM_011542840.1:c.6976-60G= (ATM)	XP_011541142.1:n.6976-60G=
XM_011542841.1:c.6976-60G= (ATM)	XP_011541143.1:n.6976-60G=
XM_011542842.1:c.6811-60G= (ATM)	XP_011541144.1:n.6811-60G=
XM_011542843.1:c.6976-60G= (ATM)	XP_011541145.1:n.6976-60G=
XM_011542844.1:c.5932-60G= (ATM)	XP_011541146.1:n.5932-60G=
XM_011542845.1:c.5668-60G= (ATM)	XP_011541147.1:n.5668-60G=
XM_011542847.1:c.2047-60G= (ATM)	XP_011541149.1:n.2047-60G=
NM_001330368.1:c.641-18514C= (C11orf65)	NP_001317297.1:n.641-18514C=
NM_001351110.1:c.*38+7635C= (C11orf65)	NP_001338039.1:n.*38+7635C=
NM_001351834.1:c.6976-60G= (ATM)	NP_001338763.1:n.6976-60G=
XM_005271562.5:c.6976-60G= (ATM)	XP_005271619.2:n.6976-60G=
XM_006718843.4:c.6976-60G= (ATM)	XP_006718906.1:n.6976-60G=
XM_006718845.2:c.2932-60G= (ATM)	XP_006718908.1:n.2932-60G=
XM_011542840.3:c.6976-60G= (ATM)	XP_011541142.1:n.6976-60G=
XM_011542842.3:c.6811-60G= (ATM)	XP_011541144.1:n.6811-60G=
XM_011542843.2:c.6976-60G= (ATM)	XP_011541145.1:n.6976-60G=
XM_011542844.3:c.5932-60G= (ATM)	XP_011541146.1:n.5932-60G=
XM_011542845.2:c.5668-60G= (ATM)	XP_011541147.1:n.5668-60G=
XM_017017789.2:c.6976-60G= (ATM)	XP_016873278.1:n.6976-60G=
XM_017017790.2:c.6976-60G= (ATM)	XP_016873279.1:n.6976-60G=
NM_001330368.2:c.641-18514C= (C11orf65)	NP_001317297.1:n.641-18514C=
NM_001351110.2:c.*38+7635C= (C11orf65)	NP_001338039.1:n.*38+7635C=
NM_001351834.2:c.6976-60G= (ATM)	NP_001338763.1:n.6976-60G=
NM_000051.4:c.6976-60G= (ATM) MANE Select	NP_000042.3:n.6976-60G=