Canonical Allele Identifier: CA476672744

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 1763196
• ClinVar RCV Id: RCV002434856
• MyVariant Identifiers: chr11:g.108214074C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108343347C>A , CM000673.2:g.108343347C>A	GRCh38
NC_000011.9:g.108214074C>A , CM000673.1:g.108214074C>A	GRCh37
NC_000011.8:g.107719284C>A	NCBI36
NG_009830.1:g.125516C>A , LRG_135:g.125516C>A
NG_054724.1:g.131486G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8394C>A (ATM)	ENSP00000388058.2:p.Ala2798=
ENST00000713593.1:c.*7865C>A (ATM)	ENSP00000518889.1:n.*7865C>A
ENST00000278616.9:c.8394C>A (ATM)	ENSP00000278616.4:p.Ala2798=
ENST00000638786.2:n.1092C>A (ATM)
ENST00000682286.1:n.3151C>A (ATM)
ENST00000682302.1:n.2812C>A (ATM)
ENST00000683174.1:n.9878C>A (ATM)
ENST00000683524.1:n.3618C>A (ATM)
ENST00000684152.1:n.3810C>A (ATM)
ENST00000684180.1:n.868C>A (ATM)
ENST00000684447.1:n.4887C>A (ATM)
ENST00000527805.6:c.*3458C>A (ATM)	ENSP00000435747.2:n.*3458C>A
ENST00000675595.1:c.*3529C>A (ATM)	ENSP00000502563.1:n.*3529C>A
ENST00000675843.1:c.8394C>A (ATM) MANE Select	ENSP00000501606.1:p.Ala2798=
ENST00000278616.8:c.8394C>A (ATM)	ENSP00000278616.4:p.Ala2798=
ENST00000452508.6:c.8394C>A (ATM)	ENSP00000388058.2:p.Ala2798=
ENST00000524755.5:c.227-8055G>T (C11orf65)
ENST00000524792.5:n.4609C>A (ATM)
ENST00000525729.5:c.641-34276G>T (C11orf65)	ENSP00000433395.1:n.641-34276G>T
ENST00000526725.1:n.272-2983G>T (C11orf65)
ENST00000527531.5:c.*1197-8055G>T (C11orf65)	ENSP00000431706.1:n.*1197-8055G>T
ENST00000615746.4:c.*1197-8055G>T (C11orf65)	ENSP00000483537.1:n.*1197-8055G>T
NM_000051.3:c.8394C>A , LRG_135t1:c.8394C>A (ATM)	NP_000042.3:p.Ala2798=
XM_005271414.3:c.788-8055G>T (C11orf65)	XP_005271471.1:n.788-8055G>T
XM_005271415.3:c.732-8055G>T (C11orf65)	XP_005271472.1:n.732-8055G>T
XM_005271561.3:c.8394C>A (ATM)	XP_005271618.2:p.Ala2798=
XM_005271562.3:c.8394C>A (ATM)	XP_005271619.2:p.Ala2798=
XM_006718843.2:c.8394C>A (ATM)	XP_006718906.1:p.Ala2798=
XM_006718845.1:c.4350C>A (ATM)	XP_006718908.1:p.Ala1450=
XM_011542640.1:c.788-2983G>T (C11orf65)	XP_011540942.1:n.788-2983G>T
XM_011542643.1:c.732-2983G>T (C11orf65)	XP_011540945.1:n.732-2983G>T
XM_011542840.1:c.8394C>A (ATM)	XP_011541142.1:p.Ala2798=
XM_011542841.1:c.8394C>A (ATM)	XP_011541143.1:p.Ala2798=
XM_011542842.1:c.8229C>A (ATM)	XP_011541144.1:p.Ala2743=
XM_011542843.1:c.8394C>A (ATM)	XP_011541145.1:p.Ala2798=
XM_011542844.1:c.7350C>A (ATM)	XP_011541146.1:p.Ala2450=
XM_011542845.1:c.7086C>A (ATM)	XP_011541147.1:p.Ala2362=
XM_011542847.1:c.3465C>A (ATM)	XP_011541149.1:p.Ala1155=
NM_001330368.1:c.641-34276G>T (C11orf65)	NP_001317297.1:n.641-34276G>T
NM_001351110.1:c.695-8055G>T (C11orf65)	NP_001338039.1:n.695-8055G>T
NM_001351834.1:c.8394C>A (ATM)	NP_001338763.1:p.Ala2798=
NR_147053.2:n.2302-8055G>T (C11orf65)
XM_005271414.4:c.788-8055G>T (C11orf65)	XP_005271471.1:n.788-8055G>T
XM_005271415.4:c.732-8055G>T (C11orf65)	XP_005271472.1:n.732-8055G>T
XM_005271562.5:c.8394C>A (ATM)	XP_005271619.2:p.Ala2798=
XM_006718843.4:c.8394C>A (ATM)	XP_006718906.1:p.Ala2798=
XM_006718845.2:c.4350C>A (ATM)	XP_006718908.1:p.Ala1450=
XM_011542640.2:c.788-2983G>T (C11orf65)	XP_011540942.1:n.788-2983G>T
XM_011542643.2:c.732-2983G>T (C11orf65)	XP_011540945.1:n.732-2983G>T
XM_011542840.3:c.8394C>A (ATM)	XP_011541142.1:p.Ala2798=
XM_011542842.3:c.8229C>A (ATM)	XP_011541144.1:p.Ala2743=
XM_011542843.2:c.8394C>A (ATM)	XP_011541145.1:p.Ala2798=
XM_011542844.3:c.7350C>A (ATM)	XP_011541146.1:p.Ala2450=
XM_011542845.2:c.7086C>A (ATM)	XP_011541147.1:p.Ala2362=
XM_017017247.1:c.904-2983G>T (C11orf65)	XP_016872736.1:n.904-2983G>T
XM_017017789.2:c.8394C>A (ATM)	XP_016873278.1:p.Ala2798=
XM_017017790.2:c.8394C>A (ATM)	XP_016873279.1:p.Ala2798=
NM_001330368.2:c.641-34276G>T (C11orf65)	NP_001317297.1:n.641-34276G>T
NM_001351110.2:c.695-8055G>T (C11orf65)	NP_001338039.1:n.695-8055G>T
NM_001351834.2:c.8394C>A (ATM)	NP_001338763.1:p.Ala2798=
NM_000051.4:c.8394C>A (ATM) MANE Select	NP_000042.3:p.Ala2798=
NR_147053.3:n.2300-8055G>T (C11orf65)