Canonical Allele Identifier: CA198094

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 187613
• ClinVar RCV Id: RCV000167357 ; RCV000550379 ; RCV003319326
• dbSNP Id: rs769142993
• ExAC: 11:108202225 G / C
• gnomAD v2: 11-108202225-G-C
• gnomAD v3: 11-108331498-G-C
• gnomAD v4: 11-108331498-G-C
• MyVariant Identifiers: chr11:g.108202225G>C (hg19) ; chr11:g.108331498G>C (hg38)
• PubMed: PMID:10980530 ; PMID:11897822 ; PMID:16622469 ; PMID:16914028 ; PMID:17166884 ; PMID:20346647 ; PMID:22071889

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108331498G>C , CM000673.2:g.108331498G>C	GRCh38
NC_000011.9:g.108202225G>C , CM000673.1:g.108202225G>C	GRCh37
NC_000011.8:g.107707435G>C	NCBI36
NG_009830.1:g.113667G>C , LRG_135:g.113667G>C
NG_054724.1:g.143335C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7570G>C (ATM)	ENSP00000388058.2:p.Ala2524Pro
ENST00000713593.1:c.*7041G>C (ATM)	ENSP00000518889.1:n.*7041G>C
ENST00000278616.9:c.7570G>C (ATM)	ENSP00000278616.4:p.Ala2524Pro
ENST00000525056.2:n.1989G>C (ATM)
ENST00000525537.3:n.527G>C (ATM)
ENST00000638786.2:n.407G>C (ATM)
ENST00000682286.1:n.2327G>C (ATM)
ENST00000682302.1:n.1988G>C (ATM)
ENST00000683174.1:n.9054G>C (ATM)
ENST00000683524.1:n.2794G>C (ATM)
ENST00000684152.1:n.3284G>C (ATM)
ENST00000684447.1:n.2033G>C (ATM)
ENST00000527805.6:c.*2634G>C (ATM)	ENSP00000435747.2:n.*2634G>C
ENST00000675595.1:c.*2705G>C (ATM)	ENSP00000502563.1:n.*2705G>C
ENST00000675843.1:c.7570G>C (ATM) MANE Select	ENSP00000501606.1:p.Ala2524Pro
ENST00000278616.8:c.7570G>C (ATM)	ENSP00000278616.4:p.Ala2524Pro
ENST00000452508.6:c.7570G>C (ATM)	ENSP00000388058.2:p.Ala2524Pro
ENST00000524755.5:c.369C>G (C11orf65)
ENST00000524792.5:n.3785G>C (ATM)
ENST00000525729.5:c.641-22427C>G (C11orf65)	ENSP00000433395.1:n.641-22427C>G
ENST00000527531.5:c.*1339C>G (C11orf65)	ENSP00000431706.1:n.*1339C>G
ENST00000533690.5:n.2974G>C (ATM)
ENST00000615746.4:c.*1339C>G (C11orf65)	ENSP00000483537.1:n.*1339C>G
NM_000051.3:c.7570G>C , LRG_135t1:c.7570G>C (ATM)	NP_000042.3:p.Ala2524Pro
XM_005271414.3:c.*108C>G (C11orf65)	XP_005271471.1:n.*108C>G
XM_005271415.3:c.*52C>G (C11orf65)	XP_005271472.1:n.*52C>G
XM_005271561.3:c.7570G>C (ATM)	XP_005271618.2:p.Ala2524Pro
XM_005271562.3:c.7570G>C (ATM)	XP_005271619.2:p.Ala2524Pro
XM_006718843.2:c.7570G>C (ATM)	XP_006718906.1:p.Ala2524Pro
XM_006718845.1:c.3526G>C (ATM)	XP_006718908.1:p.Ala1176Pro
XM_011542840.1:c.7570G>C (ATM)	XP_011541142.1:p.Ala2524Pro
XM_011542841.1:c.7570G>C (ATM)	XP_011541143.1:p.Ala2524Pro
XM_011542842.1:c.7405G>C (ATM)	XP_011541144.1:p.Ala2469Pro
XM_011542843.1:c.7570G>C (ATM)	XP_011541145.1:p.Ala2524Pro
XM_011542844.1:c.6526G>C (ATM)	XP_011541146.1:p.Ala2176Pro
XM_011542845.1:c.6262G>C (ATM)	XP_011541147.1:p.Ala2088Pro
XM_011542847.1:c.2641G>C (ATM)	XP_011541149.1:p.Ala881Pro
NM_001330368.1:c.641-22427C>G (C11orf65)	NP_001317297.1:n.641-22427C>G
NM_001351110.1:c.*38+3722C>G (C11orf65)	NP_001338039.1:n.*38+3722C>G
NM_001351834.1:c.7570G>C (ATM)	NP_001338763.1:p.Ala2524Pro
NR_147053.2:n.2444C>G (C11orf65)
XM_005271414.4:c.*108C>G (C11orf65)	XP_005271471.1:n.*108C>G
XM_005271415.4:c.*52C>G (C11orf65)	XP_005271472.1:n.*52C>G
XM_005271562.5:c.7570G>C (ATM)	XP_005271619.2:p.Ala2524Pro
XM_006718843.4:c.7570G>C (ATM)	XP_006718906.1:p.Ala2524Pro
XM_006718845.2:c.3526G>C (ATM)	XP_006718908.1:p.Ala1176Pro
XM_011542840.3:c.7570G>C (ATM)	XP_011541142.1:p.Ala2524Pro
XM_011542842.3:c.7405G>C (ATM)	XP_011541144.1:p.Ala2469Pro
XM_011542843.2:c.7570G>C (ATM)	XP_011541145.1:p.Ala2524Pro
XM_011542844.3:c.6526G>C (ATM)	XP_011541146.1:p.Ala2176Pro
XM_011542845.2:c.6262G>C (ATM)	XP_011541147.1:p.Ala2088Pro
XM_017017789.2:c.7570G>C (ATM)	XP_016873278.1:p.Ala2524Pro
XM_017017790.2:c.7570G>C (ATM)	XP_016873279.1:p.Ala2524Pro
NM_001330368.2:c.641-22427C>G (C11orf65)	NP_001317297.1:n.641-22427C>G
NM_001351110.2:c.*38+3722C>G (C11orf65)	NP_001338039.1:n.*38+3722C>G
NM_001351834.2:c.7570G>C (ATM)	NP_001338763.1:p.Ala2524Pro
NM_000051.4:c.7570G>C (ATM) MANE Select	NP_000042.3:p.Ala2524Pro
NR_147053.3:n.2442C>G (C11orf65)