Canonical Allele Identifier: CA913188485

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 629858
• ClinVar RCV Id: RCV000774649
• dbSNP Id: rs1565529987

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108330351_108330352delinsCT , CM000673.2:g.108330351_108330352delinsCT	GRCh38
NC_000011.9:g.108201078_108201079delinsCT , CM000673.1:g.108201078_108201079delinsCT	GRCh37
NC_000011.8:g.107706288_107706289delinsCT	NCBI36
NG_009830.1:g.112520_112521delinsCT , LRG_135:g.112520_112521delinsCT
NG_054724.1:g.144481_144482delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7445_7446delinsCT (ATM)	ENSP00000388058.2:p.Met2482Thr
ENST00000713593.1:c.*6916_*6917delinsCT (ATM)	ENSP00000518889.1:n.*6916_*6917delinsCT
ENST00000278616.9:c.7445_7446delinsCT (ATM)	ENSP00000278616.4:p.Met2482Thr
ENST00000525056.2:n.1864_1865delinsCT (ATM)
ENST00000525537.3:n.402_403delinsCT (ATM)
ENST00000638786.2:n.282_283delinsCT (ATM)
ENST00000682286.1:n.2202_2203delinsCT (ATM)
ENST00000682302.1:n.1863_1864delinsCT (ATM)
ENST00000683174.1:n.8929_8930delinsCT (ATM)
ENST00000683524.1:n.2669_2670delinsCT (ATM)
ENST00000684152.1:n.3159_3160delinsCT (ATM)
ENST00000684447.1:n.1908_1909delinsCT (ATM)
ENST00000527805.6:c.*2509_*2510delinsCT (ATM)	ENSP00000435747.2:n.*2509_*2510delinsCT
ENST00000675595.1:c.*2580_*2581delinsCT (ATM)	ENSP00000502563.1:n.*2580_*2581delinsCT
ENST00000675843.1:c.7445_7446delinsCT (ATM) MANE Select	ENSP00000501606.1:p.Met2482Thr
ENST00000278616.8:c.7445_7446delinsCT (ATM)	ENSP00000278616.4:p.Met2482Thr
ENST00000452508.6:c.7445_7446delinsCT (ATM)	ENSP00000388058.2:p.Met2482Thr
ENST00000524792.5:n.3660_3661delinsCT (ATM)
ENST00000525729.5:c.641-21281_641-21280delinsAG (C11orf65)	ENSP00000433395.1:n.641-21281_641-21280delinsAG
ENST00000533690.5:n.2849_2850delinsCT (ATM)
NM_000051.3:c.7445_7446delinsCT , LRG_135t1:c.7445_7446delinsCT (ATM)	NP_000042.3:p.Met2482Thr
XM_005271561.3:c.7445_7446delinsCT (ATM)	XP_005271618.2:p.Met2482Thr
XM_005271562.3:c.7445_7446delinsCT (ATM)	XP_005271619.2:p.Met2482Thr
XM_006718843.2:c.7445_7446delinsCT (ATM)	XP_006718906.1:p.Met2482Thr
XM_006718845.1:c.3401_3402delinsCT (ATM)	XP_006718908.1:p.Met1134Thr
XM_011542840.1:c.7445_7446delinsCT (ATM)	XP_011541142.1:p.Met2482Thr
XM_011542841.1:c.7445_7446delinsCT (ATM)	XP_011541143.1:p.Met2482Thr
XM_011542842.1:c.7280_7281delinsCT (ATM)	XP_011541144.1:p.Met2427Thr
XM_011542843.1:c.7445_7446delinsCT (ATM)	XP_011541145.1:p.Met2482Thr
XM_011542844.1:c.6401_6402delinsCT (ATM)	XP_011541146.1:p.Met2134Thr
XM_011542845.1:c.6137_6138delinsCT (ATM)	XP_011541147.1:p.Met2046Thr
XM_011542847.1:c.2516_2517delinsCT (ATM)	XP_011541149.1:p.Met839Thr
NM_001330368.1:c.641-21281_641-21280delinsAG (C11orf65)	NP_001317297.1:n.641-21281_641-21280delinsAG
NM_001351110.1:c.*38+4868_*38+4869delinsAG (C11orf65)	NP_001338039.1:n.*38+4868_*38+4869delinsAG
NM_001351834.1:c.7445_7446delinsCT (ATM)	NP_001338763.1:p.Met2482Thr
XM_005271562.5:c.7445_7446delinsCT (ATM)	XP_005271619.2:p.Met2482Thr
XM_006718843.4:c.7445_7446delinsCT (ATM)	XP_006718906.1:p.Met2482Thr
XM_006718845.2:c.3401_3402delinsCT (ATM)	XP_006718908.1:p.Met1134Thr
XM_011542840.3:c.7445_7446delinsCT (ATM)	XP_011541142.1:p.Met2482Thr
XM_011542842.3:c.7280_7281delinsCT (ATM)	XP_011541144.1:p.Met2427Thr
XM_011542843.2:c.7445_7446delinsCT (ATM)	XP_011541145.1:p.Met2482Thr
XM_011542844.3:c.6401_6402delinsCT (ATM)	XP_011541146.1:p.Met2134Thr
XM_011542845.2:c.6137_6138delinsCT (ATM)	XP_011541147.1:p.Met2046Thr
XM_017017789.2:c.7445_7446delinsCT (ATM)	XP_016873278.1:p.Met2482Thr
XM_017017790.2:c.7445_7446delinsCT (ATM)	XP_016873279.1:p.Met2482Thr
NM_001330368.2:c.641-21281_641-21280delinsAG (C11orf65)	NP_001317297.1:n.641-21281_641-21280delinsAG
NM_001351110.2:c.*38+4868_*38+4869delinsAG (C11orf65)	NP_001338039.1:n.*38+4868_*38+4869delinsAG
NM_001351834.2:c.7445_7446delinsCT (ATM)	NP_001338763.1:p.Met2482Thr
NM_000051.4:c.7445_7446delinsCT (ATM) MANE Select	NP_000042.3:p.Met2482Thr