Canonical Allele Identifier: CA10579202

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 234219
• ClinVar RCV Id: RCV000222930 ; RCV000235262 ; RCV000234260
• dbSNP Id: rs876660935
• gnomAD v4: 11-108312448-A-G
• MyVariant Identifiers: chr11:g.108183175A>G (hg19) ; chr11:g.108312448A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108312448A>G , CM000673.2:g.108312448A>G	GRCh38
NC_000011.9:g.108183175A>G , CM000673.1:g.108183175A>G	GRCh37
NC_000011.8:g.107688385A>G	NCBI36
NG_009830.1:g.94617A>G , LRG_135:g.94617A>G
NG_054724.1:g.162385T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5956A>G (ATM)	ENSP00000388058.2:p.Ile1986Val
ENST00000713593.1:c.*5427A>G (ATM)	ENSP00000518889.1:n.*5427A>G
ENST00000278616.9:c.5956A>G (ATM)	ENSP00000278616.4:p.Ile1986Val
ENST00000525056.2:n.375A>G (ATM)
ENST00000682286.1:n.713A>G (ATM)
ENST00000682302.1:n.374A>G (ATM)
ENST00000683174.1:n.7440A>G (ATM)
ENST00000683524.1:n.1180A>G (ATM)
ENST00000684152.1:n.1670A>G (ATM)
ENST00000527805.6:c.*1020A>G (ATM)	ENSP00000435747.2:n.*1020A>G
ENST00000675595.1:c.*1020A>G (ATM)	ENSP00000502563.1:n.*1020A>G
ENST00000675843.1:c.5956A>G (ATM) MANE Select	ENSP00000501606.1:p.Ile1986Val
ENST00000278616.8:c.5956A>G (ATM)	ENSP00000278616.4:p.Ile1986Val
ENST00000452508.6:c.5956A>G (ATM)	ENSP00000388058.2:p.Ile1986Val
ENST00000524792.5:n.2171A>G (ATM)
ENST00000525729.5:c.641-3377T>C (C11orf65)	ENSP00000433395.1:n.641-3377T>C
ENST00000529588.5:c.380A>G (ATM)
ENST00000532765.1:n.273A>G (ATM)
ENST00000533690.5:n.1360A>G (ATM)
NM_000051.3:c.5956A>G , LRG_135t1:c.5956A>G (ATM)	NP_000042.3:p.Ile1986Val
XM_005271561.3:c.5956A>G (ATM)	XP_005271618.2:p.Ile1986Val
XM_005271562.3:c.5956A>G (ATM)	XP_005271619.2:p.Ile1986Val
XM_006718843.2:c.5956A>G (ATM)	XP_006718906.1:p.Ile1986Val
XM_006718845.1:c.1912A>G (ATM)	XP_006718908.1:p.Ile638Val
XM_011542840.1:c.5956A>G (ATM)	XP_011541142.1:p.Ile1986Val
XM_011542841.1:c.5956A>G (ATM)	XP_011541143.1:p.Ile1986Val
XM_011542842.1:c.5791A>G (ATM)	XP_011541144.1:p.Ile1931Val
XM_011542843.1:c.5956A>G (ATM)	XP_011541145.1:p.Ile1986Val
XM_011542844.1:c.4912A>G (ATM)	XP_011541146.1:p.Ile1638Val
XM_011542845.1:c.4648A>G (ATM)	XP_011541147.1:p.Ile1550Val
XM_011542847.1:c.1027A>G (ATM)	XP_011541149.1:p.Ile343Val
NM_001330368.1:c.641-3377T>C (C11orf65)	NP_001317297.1:n.641-3377T>C
NM_001351110.1:c.*39-3377T>C (C11orf65)	NP_001338039.1:n.*39-3377T>C
NM_001351834.1:c.5956A>G (ATM)	NP_001338763.1:p.Ile1986Val
XM_005271562.5:c.5956A>G (ATM)	XP_005271619.2:p.Ile1986Val
XM_006718843.4:c.5956A>G (ATM)	XP_006718906.1:p.Ile1986Val
XM_006718845.2:c.1912A>G (ATM)	XP_006718908.1:p.Ile638Val
XM_011542840.3:c.5956A>G (ATM)	XP_011541142.1:p.Ile1986Val
XM_011542842.3:c.5791A>G (ATM)	XP_011541144.1:p.Ile1931Val
XM_011542843.2:c.5956A>G (ATM)	XP_011541145.1:p.Ile1986Val
XM_011542844.3:c.4912A>G (ATM)	XP_011541146.1:p.Ile1638Val
XM_011542845.2:c.4648A>G (ATM)	XP_011541147.1:p.Ile1550Val
XM_017017789.2:c.5956A>G (ATM)	XP_016873278.1:p.Ile1986Val
XM_017017790.2:c.5956A>G (ATM)	XP_016873279.1:p.Ile1986Val
XM_017017791.1:c.5956A>G (ATM)	XP_016873280.1:p.Ile1986Val
XR_002957150.1:n.6556A>G (ATM)
NM_001330368.2:c.641-3377T>C (C11orf65)	NP_001317297.1:n.641-3377T>C
NM_001351110.2:c.*39-3377T>C (C11orf65)	NP_001338039.1:n.*39-3377T>C
NM_001351834.2:c.5956A>G (ATM)	NP_001338763.1:p.Ile1986Val
NM_000051.4:c.5956A>G (ATM) MANE Select	NP_000042.3:p.Ile1986Val