Canonical Allele Identifier: CA6266177

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 453703
• ClinVar RCV Id: RCV000776302 ; RCV000554985 ; RCV000606073
• dbSNP Id: rs749610251
• ExAC: 11:108202771 G / A
• gnomAD v2: 11-108202771-G-A
• gnomAD v4: 11-108332044-G-A
• MyVariant Identifiers: chr11:g.108202771G>A (hg19) ; chr11:g.108332044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108332044G>A , CM000673.2:g.108332044G>A	GRCh38
NC_000011.9:g.108202771G>A , CM000673.1:g.108202771G>A	GRCh37
NC_000011.8:g.107707981G>A	NCBI36
NG_009830.1:g.114213G>A , LRG_135:g.114213G>A
NG_054724.1:g.142789C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7788+7G>A (ATM)	ENSP00000388058.2:n.7788+7G>A
ENST00000713593.1:c.*7259+7G>A (ATM)	ENSP00000518889.1:n.*7259+7G>A
ENST00000278616.9:c.7788+7G>A (ATM)	ENSP00000278616.4:n.7788+7G>A
ENST00000525056.2:n.2207+7G>A (ATM)
ENST00000525537.3:n.752G>A (ATM)
ENST00000638786.2:n.625+7G>A (ATM)
ENST00000682286.1:n.2545+7G>A (ATM)
ENST00000682302.1:n.2206+7G>A (ATM)
ENST00000683174.1:n.9272+7G>A (ATM)
ENST00000683524.1:n.3012+7G>A (ATM)
ENST00000684152.1:n.3343+487G>A (ATM)
ENST00000684447.1:n.2579G>A (ATM)
ENST00000527805.6:c.*2852+7G>A (ATM)	ENSP00000435747.2:n.*2852+7G>A
ENST00000675595.1:c.*2923+7G>A (ATM)	ENSP00000502563.1:n.*2923+7G>A
ENST00000675843.1:c.7788+7G>A (ATM) MANE Select	ENSP00000501606.1:n.7788+7G>A
ENST00000278616.8:c.7788+7G>A (ATM)	ENSP00000278616.4:n.7788+7G>A
ENST00000452508.6:c.7788+7G>A (ATM)	ENSP00000388058.2:n.7788+7G>A
ENST00000524755.5:c.300-477C>T (C11orf65)
ENST00000524792.5:n.4003+7G>A (ATM)
ENST00000525729.5:c.641-22973C>T (C11orf65)	ENSP00000433395.1:n.641-22973C>T
ENST00000527531.5:c.*1270-477C>T (C11orf65)	ENSP00000431706.1:n.*1270-477C>T
ENST00000533690.5:n.3192+7G>A (ATM)
ENST00000615746.4:c.*1270-477C>T (C11orf65)	ENSP00000483537.1:n.*1270-477C>T
NM_000051.3:c.7788+7G>A , LRG_135t1:c.7788+7G>A (ATM)	NP_000042.3:n.7788+7G>A
XM_005271414.3:c.*39-477C>T (C11orf65)	XP_005271471.1:n.*39-477C>T
XM_005271415.3:c.805-477C>T (C11orf65)	XP_005271472.1:n.805-477C>T
XM_005271561.3:c.7788+7G>A (ATM)	XP_005271618.2:n.7788+7G>A
XM_005271562.3:c.7788+7G>A (ATM)	XP_005271619.2:n.7788+7G>A
XM_006718843.2:c.7788+7G>A (ATM)	XP_006718906.1:n.7788+7G>A
XM_006718845.1:c.3744+7G>A (ATM)	XP_006718908.1:n.3744+7G>A
XM_011542840.1:c.7788+7G>A (ATM)	XP_011541142.1:n.7788+7G>A
XM_011542841.1:c.7788+7G>A (ATM)	XP_011541143.1:n.7788+7G>A
XM_011542842.1:c.7623+7G>A (ATM)	XP_011541144.1:n.7623+7G>A
XM_011542843.1:c.7788+7G>A (ATM)	XP_011541145.1:n.7788+7G>A
XM_011542844.1:c.6744+7G>A (ATM)	XP_011541146.1:n.6744+7G>A
XM_011542845.1:c.6480+7G>A (ATM)	XP_011541147.1:n.6480+7G>A
XM_011542847.1:c.2859+7G>A (ATM)	XP_011541149.1:n.2859+7G>A
NM_001330368.1:c.641-22973C>T (C11orf65)	NP_001317297.1:n.641-22973C>T
NM_001351110.1:c.*38+3176C>T (C11orf65)	NP_001338039.1:n.*38+3176C>T
NM_001351834.1:c.7788+7G>A (ATM)	NP_001338763.1:n.7788+7G>A
NR_147053.2:n.2375-477C>T (C11orf65)
XM_005271414.4:c.*39-477C>T (C11orf65)	XP_005271471.1:n.*39-477C>T
XM_005271415.4:c.805-477C>T (C11orf65)	XP_005271472.1:n.805-477C>T
XM_005271562.5:c.7788+7G>A (ATM)	XP_005271619.2:n.7788+7G>A
XM_006718843.4:c.7788+7G>A (ATM)	XP_006718906.1:n.7788+7G>A
XM_006718845.2:c.3744+7G>A (ATM)	XP_006718908.1:n.3744+7G>A
XM_011542840.3:c.7788+7G>A (ATM)	XP_011541142.1:n.7788+7G>A
XM_011542842.3:c.7623+7G>A (ATM)	XP_011541144.1:n.7623+7G>A
XM_011542843.2:c.7788+7G>A (ATM)	XP_011541145.1:n.7788+7G>A
XM_011542844.3:c.6744+7G>A (ATM)	XP_011541146.1:n.6744+7G>A
XM_011542845.2:c.6480+7G>A (ATM)	XP_011541147.1:n.6480+7G>A
XM_017017789.2:c.7788+7G>A (ATM)	XP_016873278.1:n.7788+7G>A
XM_017017790.2:c.7788+7G>A (ATM)	XP_016873279.1:n.7788+7G>A
NM_001330368.2:c.641-22973C>T (C11orf65)	NP_001317297.1:n.641-22973C>T
NM_001351110.2:c.*38+3176C>T (C11orf65)	NP_001338039.1:n.*38+3176C>T
NM_001351834.2:c.7788+7G>A (ATM)	NP_001338763.1:n.7788+7G>A
NM_000051.4:c.7788+7G>A (ATM) MANE Select	NP_000042.3:n.7788+7G>A
NR_147053.3:n.2373-477C>T (C11orf65)