Canonical Allele Identifier: CA913189711

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 617781
• ClinVar RCV Id: RCV000755037 ; RCV001231387 ; RCV002467452
• dbSNP Id: rs1565499093

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108315898del , CM000673.2:g.108315898del	GRCh38
NC_000011.9:g.108186625del , CM000673.1:g.108186625del	GRCh37
NC_000011.8:g.107691835del	NCBI36
NG_009830.1:g.98067del , LRG_135:g.98067del
NG_054724.1:g.158935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6082del (ATM)	ENSP00000388058.2:p.Gln2028AsnfsTer19
ENST00000713593.1:c.*5553del (ATM)	ENSP00000518889.1:n.*5553del
ENST00000278616.9:c.6082del (ATM)	ENSP00000278616.4:p.Gln2028AsnfsTer19
ENST00000525056.2:n.501del (ATM)
ENST00000682286.1:n.839del (ATM)
ENST00000682302.1:n.500del (ATM)
ENST00000683174.1:n.7566del (ATM)
ENST00000683524.1:n.1306del (ATM)
ENST00000684152.1:n.1796del (ATM)
ENST00000527805.6:c.*1146del (ATM)	ENSP00000435747.2:n.*1146del
ENST00000675595.1:c.*1146del (ATM)	ENSP00000502563.1:n.*1146del
ENST00000675843.1:c.6082del (ATM) MANE Select	ENSP00000501606.1:p.Gln2028AsnfsTer19
ENST00000278616.8:c.6082del (ATM)	ENSP00000278616.4:p.Gln2028AsnfsTer19
ENST00000452508.6:c.6082del (ATM)	ENSP00000388058.2:p.Gln2028AsnfsTer19
ENST00000524792.5:n.2297del (ATM)
ENST00000525729.5:c.641-6827del (C11orf65)	ENSP00000433395.1:n.641-6827del
ENST00000532765.1:n.399del (ATM)
ENST00000533690.5:n.1486del (ATM)
NM_000051.3:c.6082del , LRG_135t1:c.6082del (ATM)	NP_000042.3:p.Gln2028AsnfsTer19
XM_005271561.3:c.6082del (ATM)	XP_005271618.2:p.Gln2028AsnfsTer19
XM_005271562.3:c.6082del (ATM)	XP_005271619.2:p.Gln2028AsnfsTer19
XM_006718843.2:c.6082del (ATM)	XP_006718906.1:p.Gln2028AsnfsTer19
XM_006718845.1:c.2038del (ATM)	XP_006718908.1:p.Gln680AsnfsTer19
XM_011542840.1:c.6082del (ATM)	XP_011541142.1:p.Gln2028AsnfsTer19
XM_011542841.1:c.6082del (ATM)	XP_011541143.1:p.Gln2028AsnfsTer19
XM_011542842.1:c.5917del (ATM)	XP_011541144.1:p.Gln1973AsnfsTer19
XM_011542843.1:c.6082del (ATM)	XP_011541145.1:p.Gln2028AsnfsTer19
XM_011542844.1:c.5038del (ATM)	XP_011541146.1:p.Gln1680AsnfsTer19
XM_011542845.1:c.4774del (ATM)	XP_011541147.1:p.Gln1592AsnfsTer19
XM_011542847.1:c.1153del (ATM)	XP_011541149.1:p.Gln385AsnfsTer19
NM_001330368.1:c.641-6827del (C11orf65)	NP_001317297.1:n.641-6827del
NM_001351110.1:c.*39-6827del (C11orf65)	NP_001338039.1:n.*39-6827del
NM_001351834.1:c.6082del (ATM)	NP_001338763.1:p.Gln2028AsnfsTer19
XM_005271562.5:c.6082del (ATM)	XP_005271619.2:p.Gln2028AsnfsTer19
XM_006718843.4:c.6082del (ATM)	XP_006718906.1:p.Gln2028AsnfsTer19
XM_006718845.2:c.2038del (ATM)	XP_006718908.1:p.Gln680AsnfsTer19
XM_011542840.3:c.6082del (ATM)	XP_011541142.1:p.Gln2028AsnfsTer19
XM_011542842.3:c.5917del (ATM)	XP_011541144.1:p.Gln1973AsnfsTer19
XM_011542843.2:c.6082del (ATM)	XP_011541145.1:p.Gln2028AsnfsTer19
XM_011542844.3:c.5038del (ATM)	XP_011541146.1:p.Gln1680AsnfsTer19
XM_011542845.2:c.4774del (ATM)	XP_011541147.1:p.Gln1592AsnfsTer19
XM_017017789.2:c.6082del (ATM)	XP_016873278.1:p.Gln2028AsnfsTer19
XM_017017790.2:c.6082del (ATM)	XP_016873279.1:p.Gln2028AsnfsTer19
XM_017017791.1:c.6082del (ATM)	XP_016873280.1:p.Gln2028AsnfsTer19
NM_001330368.2:c.641-6827del (C11orf65)	NP_001317297.1:n.641-6827del
NM_001351110.2:c.*39-6827del (C11orf65)	NP_001338039.1:n.*39-6827del
NM_001351834.2:c.6082del (ATM)	NP_001338763.1:p.Gln2028AsnfsTer19
NM_000051.4:c.6082del (ATM) MANE Select	NP_000042.3:p.Gln2028AsnfsTer19