Canonical Allele Identifier: CA228402813
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1276077
ClinVar RCV Id: RCV001694402
dbSNP Id: rs113573757

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108317102_108317103insA , CM000673.2:g.108317102_108317103insA GRCh38
NC_000011.9:g.108187829_108187830insA , CM000673.1:g.108187829_108187830insA GRCh37
NC_000011.8:g.107693039_107693040insA NCBI36
NG_009830.1:g.99271_99272insA , LRG_135:g.99271_99272insA
NG_054724.1:g.157730_157731insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.6199-271_6199-270insA (ATM) ENSP00000388058.2:n.6199-271_6199-270insA
ENST00000713593.1:c.*5670-271_*5670-270insA (ATM) ENSP00000518889.1:n.*5670-271_*5670-270insA
ENST00000278616.9:c.6199-271_6199-270insA (ATM) ENSP00000278616.4:n.6199-271_6199-270insA
ENST00000525056.2:n.618-271_618-270insA (ATM)
ENST00000682286.1:n.956-271_956-270insA (ATM)
ENST00000682302.1:n.617-271_617-270insA (ATM)
ENST00000683174.1:n.7683-271_7683-270insA (ATM)
ENST00000683524.1:n.1423-271_1423-270insA (ATM)
ENST00000684152.1:n.1913-271_1913-270insA (ATM)
ENST00000527805.6:c.*1263-271_*1263-270insA (ATM) ENSP00000435747.2:n.*1263-271_*1263-270insA
ENST00000675595.1:c.*1263-271_*1263-270insA (ATM) ENSP00000502563.1:n.*1263-271_*1263-270insA
ENST00000675843.1:c.6199-271_6199-270insA (ATM) MANE Select ENSP00000501606.1:n.6199-271_6199-270insA
ENST00000278616.8:c.6199-271_6199-270insA (ATM) ENSP00000278616.4:n.6199-271_6199-270insA
ENST00000452508.6:c.6199-271_6199-270insA (ATM) ENSP00000388058.2:n.6199-271_6199-270insA
ENST00000524792.5:n.2414-271_2414-270insA (ATM)
ENST00000525729.5:c.641-8032_641-8031insT (C11orf65) ENSP00000433395.1:n.641-8032_641-8031insT
ENST00000532765.1:n.516-271_516-270insA (ATM)
ENST00000533690.5:n.1603-271_1603-270insA (ATM)
NM_000051.3:c.6199-271_6199-270insA , LRG_135t1:c.6199-271_6199-270insA (ATM) NP_000042.3:n.6199-271_6199-270insA
XM_005271561.3:c.6199-271_6199-270insA (ATM) XP_005271618.2:n.6199-271_6199-270insA
XM_005271562.3:c.6199-271_6199-270insA (ATM) XP_005271619.2:n.6199-271_6199-270insA
XM_006718843.2:c.6199-271_6199-270insA (ATM) XP_006718906.1:n.6199-271_6199-270insA
XM_006718845.1:c.2155-271_2155-270insA (ATM) XP_006718908.1:n.2155-271_2155-270insA
XM_011542840.1:c.6199-271_6199-270insA (ATM) XP_011541142.1:n.6199-271_6199-270insA
XM_011542841.1:c.6199-271_6199-270insA (ATM) XP_011541143.1:n.6199-271_6199-270insA
XM_011542842.1:c.6034-271_6034-270insA (ATM) XP_011541144.1:n.6034-271_6034-270insA
XM_011542843.1:c.6199-271_6199-270insA (ATM) XP_011541145.1:n.6199-271_6199-270insA
XM_011542844.1:c.5155-271_5155-270insA (ATM) XP_011541146.1:n.5155-271_5155-270insA
XM_011542845.1:c.4891-271_4891-270insA (ATM) XP_011541147.1:n.4891-271_4891-270insA
XM_011542847.1:c.1270-271_1270-270insA (ATM) XP_011541149.1:n.1270-271_1270-270insA
NM_001330368.1:c.641-8032_641-8031insT (C11orf65) NP_001317297.1:n.641-8032_641-8031insT
NM_001351110.1:c.*39-8032_*39-8031insT (C11orf65) NP_001338039.1:n.*39-8032_*39-8031insT
NM_001351834.1:c.6199-271_6199-270insA (ATM) NP_001338763.1:n.6199-271_6199-270insA
XM_005271562.5:c.6199-271_6199-270insA (ATM) XP_005271619.2:n.6199-271_6199-270insA
XM_006718843.4:c.6199-271_6199-270insA (ATM) XP_006718906.1:n.6199-271_6199-270insA
XM_006718845.2:c.2155-271_2155-270insA (ATM) XP_006718908.1:n.2155-271_2155-270insA
XM_011542840.3:c.6199-271_6199-270insA (ATM) XP_011541142.1:n.6199-271_6199-270insA
XM_011542842.3:c.6034-271_6034-270insA (ATM) XP_011541144.1:n.6034-271_6034-270insA
XM_011542843.2:c.6199-271_6199-270insA (ATM) XP_011541145.1:n.6199-271_6199-270insA
XM_011542844.3:c.5155-271_5155-270insA (ATM) XP_011541146.1:n.5155-271_5155-270insA
XM_011542845.2:c.4891-271_4891-270insA (ATM) XP_011541147.1:n.4891-271_4891-270insA
XM_017017789.2:c.6199-271_6199-270insA (ATM) XP_016873278.1:n.6199-271_6199-270insA
XM_017017790.2:c.6199-271_6199-270insA (ATM) XP_016873279.1:n.6199-271_6199-270insA
XM_017017791.1:c.6199-271_6199-270insA (ATM) XP_016873280.1:n.6199-271_6199-270insA
NM_001330368.2:c.641-8032_641-8031insT (C11orf65) NP_001317297.1:n.641-8032_641-8031insT
NM_001351110.2:c.*39-8032_*39-8031insT (C11orf65) NP_001338039.1:n.*39-8032_*39-8031insT
NM_001351834.2:c.6199-271_6199-270insA (ATM) NP_001338763.1:n.6199-271_6199-270insA
NM_000051.4:c.6199-271_6199-270insA (ATM) MANE Select NP_000042.3:n.6199-271_6199-270insA