Canonical Allele Identifier: CA476672769

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 1668025
• ClinVar RCV Id: RCV002195890
• dbSNP Id: rs2136952999
• MyVariant Identifiers: chr11:g.108214086A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108343359A>G , CM000673.2:g.108343359A>G	GRCh38
NC_000011.9:g.108214086A>G , CM000673.1:g.108214086A>G	GRCh37
NC_000011.8:g.107719296A>G	NCBI36
NG_009830.1:g.125528A>G , LRG_135:g.125528A>G
NG_054724.1:g.131474T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.8406A>G (ATM)	ENSP00000388058.2:p.Gln2802=
ENST00000713593.1:c.*7877A>G (ATM)	ENSP00000518889.1:n.*7877A>G
ENST00000278616.9:c.8406A>G (ATM)	ENSP00000278616.4:p.Gln2802=
ENST00000638786.2:n.1104A>G (ATM)
ENST00000682286.1:n.3163A>G (ATM)
ENST00000682302.1:n.2824A>G (ATM)
ENST00000683174.1:n.9890A>G (ATM)
ENST00000683524.1:n.3630A>G (ATM)
ENST00000684152.1:n.3822A>G (ATM)
ENST00000684180.1:n.880A>G (ATM)
ENST00000684447.1:n.4899A>G (ATM)
ENST00000527805.6:c.*3470A>G (ATM)	ENSP00000435747.2:n.*3470A>G
ENST00000675595.1:c.*3541A>G (ATM)	ENSP00000502563.1:n.*3541A>G
ENST00000675843.1:c.8406A>G (ATM) MANE Select	ENSP00000501606.1:p.Gln2802=
ENST00000278616.8:c.8406A>G (ATM)	ENSP00000278616.4:p.Gln2802=
ENST00000452508.6:c.8406A>G (ATM)	ENSP00000388058.2:p.Gln2802=
ENST00000524755.5:c.227-8067T>C (C11orf65)
ENST00000524792.5:n.4621A>G (ATM)
ENST00000525729.5:c.641-34288T>C (C11orf65)	ENSP00000433395.1:n.641-34288T>C
ENST00000526725.1:n.272-2995T>C (C11orf65)
ENST00000527531.5:c.*1197-8067T>C (C11orf65)	ENSP00000431706.1:n.*1197-8067T>C
ENST00000615746.4:c.*1197-8067T>C (C11orf65)	ENSP00000483537.1:n.*1197-8067T>C
NM_000051.3:c.8406A>G , LRG_135t1:c.8406A>G (ATM)	NP_000042.3:p.Gln2802=
XM_005271414.3:c.788-8067T>C (C11orf65)	XP_005271471.1:n.788-8067T>C
XM_005271415.3:c.732-8067T>C (C11orf65)	XP_005271472.1:n.732-8067T>C
XM_005271561.3:c.8406A>G (ATM)	XP_005271618.2:p.Gln2802=
XM_005271562.3:c.8406A>G (ATM)	XP_005271619.2:p.Gln2802=
XM_006718843.2:c.8406A>G (ATM)	XP_006718906.1:p.Gln2802=
XM_006718845.1:c.4362A>G (ATM)	XP_006718908.1:p.Gln1454=
XM_011542640.1:c.788-2995T>C (C11orf65)	XP_011540942.1:n.788-2995T>C
XM_011542643.1:c.732-2995T>C (C11orf65)	XP_011540945.1:n.732-2995T>C
XM_011542840.1:c.8406A>G (ATM)	XP_011541142.1:p.Gln2802=
XM_011542841.1:c.8406A>G (ATM)	XP_011541143.1:p.Gln2802=
XM_011542842.1:c.8241A>G (ATM)	XP_011541144.1:p.Gln2747=
XM_011542843.1:c.8406A>G (ATM)	XP_011541145.1:p.Gln2802=
XM_011542844.1:c.7362A>G (ATM)	XP_011541146.1:p.Gln2454=
XM_011542845.1:c.7098A>G (ATM)	XP_011541147.1:p.Gln2366=
XM_011542847.1:c.3477A>G (ATM)	XP_011541149.1:p.Gln1159=
NM_001330368.1:c.641-34288T>C (C11orf65)	NP_001317297.1:n.641-34288T>C
NM_001351110.1:c.695-8067T>C (C11orf65)	NP_001338039.1:n.695-8067T>C
NM_001351834.1:c.8406A>G (ATM)	NP_001338763.1:p.Gln2802=
NR_147053.2:n.2302-8067T>C (C11orf65)
XM_005271414.4:c.788-8067T>C (C11orf65)	XP_005271471.1:n.788-8067T>C
XM_005271415.4:c.732-8067T>C (C11orf65)	XP_005271472.1:n.732-8067T>C
XM_005271562.5:c.8406A>G (ATM)	XP_005271619.2:p.Gln2802=
XM_006718843.4:c.8406A>G (ATM)	XP_006718906.1:p.Gln2802=
XM_006718845.2:c.4362A>G (ATM)	XP_006718908.1:p.Gln1454=
XM_011542640.2:c.788-2995T>C (C11orf65)	XP_011540942.1:n.788-2995T>C
XM_011542643.2:c.732-2995T>C (C11orf65)	XP_011540945.1:n.732-2995T>C
XM_011542840.3:c.8406A>G (ATM)	XP_011541142.1:p.Gln2802=
XM_011542842.3:c.8241A>G (ATM)	XP_011541144.1:p.Gln2747=
XM_011542843.2:c.8406A>G (ATM)	XP_011541145.1:p.Gln2802=
XM_011542844.3:c.7362A>G (ATM)	XP_011541146.1:p.Gln2454=
XM_011542845.2:c.7098A>G (ATM)	XP_011541147.1:p.Gln2366=
XM_017017247.1:c.904-2995T>C (C11orf65)	XP_016872736.1:n.904-2995T>C
XM_017017789.2:c.8406A>G (ATM)	XP_016873278.1:p.Gln2802=
XM_017017790.2:c.8406A>G (ATM)	XP_016873279.1:p.Gln2802=
NM_001330368.2:c.641-34288T>C (C11orf65)	NP_001317297.1:n.641-34288T>C
NM_001351110.2:c.695-8067T>C (C11orf65)	NP_001338039.1:n.695-8067T>C
NM_001351834.2:c.8406A>G (ATM)	NP_001338763.1:p.Gln2802=
NM_000051.4:c.8406A>G (ATM) MANE Select	NP_000042.3:p.Gln2802=
NR_147053.3:n.2300-8067T>C (C11orf65)