Canonical Allele Identifier: CA916080489

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 863320
• ClinVar RCV Id: RCV001070260
• dbSNP Id: rs2085567158

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108325437del , CM000673.2:g.108325437del	GRCh38
NC_000011.9:g.108196164del , CM000673.1:g.108196164del	GRCh37
NC_000011.8:g.107701374del	NCBI36
NG_009830.1:g.107606del , LRG_135:g.107606del
NG_054724.1:g.149397del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6700del (ATM)	ENSP00000388058.2:p.Leu2234Ter
ENST00000713593.1:c.*6171del (ATM)	ENSP00000518889.1:n.*6171del
ENST00000278616.9:c.6700del (ATM)	ENSP00000278616.4:p.Leu2234Ter
ENST00000525056.2:n.1119del (ATM)
ENST00000682286.1:n.1457del (ATM)
ENST00000682302.1:n.1118del (ATM)
ENST00000683174.1:n.8184del (ATM)
ENST00000683524.1:n.1924del (ATM)
ENST00000684152.1:n.2414del (ATM)
ENST00000527805.6:c.*1764del (ATM)	ENSP00000435747.2:n.*1764del
ENST00000675595.1:c.*1835del (ATM)	ENSP00000502563.1:n.*1835del
ENST00000675843.1:c.6700del (ATM) MANE Select	ENSP00000501606.1:p.Leu2234Ter
ENST00000278616.8:c.6700del (ATM)	ENSP00000278616.4:p.Leu2234Ter
ENST00000452508.6:c.6700del (ATM)	ENSP00000388058.2:p.Leu2234Ter
ENST00000524792.5:n.2915del (ATM)
ENST00000525729.5:c.641-16365del (C11orf65)	ENSP00000433395.1:n.641-16365del
ENST00000533690.5:n.2104del (ATM)
NM_000051.3:c.6700del , LRG_135t1:c.6700del (ATM)	NP_000042.3:p.Leu2234Ter
XM_005271561.3:c.6700del (ATM)	XP_005271618.2:p.Leu2234Ter
XM_005271562.3:c.6700del (ATM)	XP_005271619.2:p.Leu2234Ter
XM_006718843.2:c.6700del (ATM)	XP_006718906.1:p.Leu2234Ter
XM_006718845.1:c.2656del (ATM)	XP_006718908.1:p.Leu886Ter
XM_011542840.1:c.6700del (ATM)	XP_011541142.1:p.Leu2234Ter
XM_011542841.1:c.6700del (ATM)	XP_011541143.1:p.Leu2234Ter
XM_011542842.1:c.6535del (ATM)	XP_011541144.1:p.Leu2179Ter
XM_011542843.1:c.6700del (ATM)	XP_011541145.1:p.Leu2234Ter
XM_011542844.1:c.5656del (ATM)	XP_011541146.1:p.Leu1886Ter
XM_011542845.1:c.5392del (ATM)	XP_011541147.1:p.Leu1798Ter
XM_011542847.1:c.1771del (ATM)	XP_011541149.1:p.Leu591Ter
NM_001330368.1:c.641-16365del (C11orf65)	NP_001317297.1:n.641-16365del
NM_001351110.1:c.*38+9784del (C11orf65)	NP_001338039.1:n.*38+9784del
NM_001351834.1:c.6700del (ATM)	NP_001338763.1:p.Leu2234Ter
XM_005271562.5:c.6700del (ATM)	XP_005271619.2:p.Leu2234Ter
XM_006718843.4:c.6700del (ATM)	XP_006718906.1:p.Leu2234Ter
XM_006718845.2:c.2656del (ATM)	XP_006718908.1:p.Leu886Ter
XM_011542840.3:c.6700del (ATM)	XP_011541142.1:p.Leu2234Ter
XM_011542842.3:c.6535del (ATM)	XP_011541144.1:p.Leu2179Ter
XM_011542843.2:c.6700del (ATM)	XP_011541145.1:p.Leu2234Ter
XM_011542844.3:c.5656del (ATM)	XP_011541146.1:p.Leu1886Ter
XM_011542845.2:c.5392del (ATM)	XP_011541147.1:p.Leu1798Ter
XM_017017789.2:c.6700del (ATM)	XP_016873278.1:p.Leu2234Ter
XM_017017790.2:c.6700del (ATM)	XP_016873279.1:p.Leu2234Ter
NM_001330368.2:c.641-16365del (C11orf65)	NP_001317297.1:n.641-16365del
NM_001351110.2:c.*38+9784del (C11orf65)	NP_001338039.1:n.*38+9784del
NM_001351834.2:c.6700del (ATM)	NP_001338763.1:p.Leu2234Ter
NM_000051.4:c.6700del (ATM) MANE Select	NP_000042.3:p.Leu2234Ter