Canonical Allele Identifier: CA10588507
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

ClinVar Variation Id: 265653
ClinVar RCV Id: RCV000255471
dbSNP Id: rs886039701

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108326116_108326117del , CM000673.2:g.108326116_108326117del GRCh38
NC_000011.9:g.108196843_108196844del , CM000673.1:g.108196843_108196844del GRCh37
NC_000011.8:g.107702053_107702054del NCBI36
NG_009830.1:g.108285_108286del , LRG_135:g.108285_108286del
NG_054724.1:g.148719_148720del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.6866_6867del (ATM) ENSP00000388058.2:p.Ser2289Ter
ENST00000713593.1:c.*6337_*6338del (ATM) ENSP00000518889.1:n.*6337_*6338del
ENST00000278616.9:c.6866_6867del (ATM) ENSP00000278616.4:p.Ser2289Ter
ENST00000525056.2:n.1285_1286del (ATM)
ENST00000682286.1:n.1623_1624del (ATM)
ENST00000682302.1:n.1284_1285del (ATM)
ENST00000683174.1:n.8350_8351del (ATM)
ENST00000683524.1:n.2090_2091del (ATM)
ENST00000684152.1:n.2580_2581del (ATM)
ENST00000527805.6:c.*1930_*1931del (ATM) ENSP00000435747.2:n.*1930_*1931del
ENST00000675595.1:c.*2001_*2002del (ATM) ENSP00000502563.1:n.*2001_*2002del
ENST00000675843.1:c.6866_6867del (ATM) MANE Select ENSP00000501606.1:p.Ser2289Ter
ENST00000278616.8:c.6866_6867del (ATM) ENSP00000278616.4:p.Ser2289Ter
ENST00000452508.6:c.6866_6867del (ATM) ENSP00000388058.2:p.Ser2289Ter
ENST00000524792.5:n.3081_3082del (ATM)
ENST00000525729.5:c.641-17043_641-17042del (C11orf65) ENSP00000433395.1:n.641-17043_641-17042de...
ENST00000533690.5:n.2270_2271del (ATM)
NM_000051.3:c.6866_6867del , LRG_135t1:c.6866_6867del (ATM) NP_000042.3:p.Ser2289Ter
XM_005271561.3:c.6866_6867del (ATM) XP_005271618.2:p.Ser2289Ter
XM_005271562.3:c.6866_6867del (ATM) XP_005271619.2:p.Ser2289Ter
XM_006718843.2:c.6866_6867del (ATM) XP_006718906.1:p.Ser2289Ter
XM_006718845.1:c.2822_2823del (ATM) XP_006718908.1:p.Ser941Ter
XM_011542840.1:c.6866_6867del (ATM) XP_011541142.1:p.Ser2289Ter
XM_011542841.1:c.6866_6867del (ATM) XP_011541143.1:p.Ser2289Ter
XM_011542842.1:c.6701_6702del (ATM) XP_011541144.1:p.Ser2234Ter
XM_011542843.1:c.6866_6867del (ATM) XP_011541145.1:p.Ser2289Ter
XM_011542844.1:c.5822_5823del (ATM) XP_011541146.1:p.Ser1941Ter
XM_011542845.1:c.5558_5559del (ATM) XP_011541147.1:p.Ser1853Ter
XM_011542847.1:c.1937_1938del (ATM) XP_011541149.1:p.Ser646Ter
NM_001330368.1:c.641-17043_641-17042del (C11orf65) NP_001317297.1:n.641-17043_641-17042del
NM_001351110.1:c.*38+9106_*38+9107del (C11orf65) NP_001338039.1:n.*38+9106_*38+9107del
NM_001351834.1:c.6866_6867del (ATM) NP_001338763.1:p.Ser2289Ter
XM_005271562.5:c.6866_6867del (ATM) XP_005271619.2:p.Ser2289Ter
XM_006718843.4:c.6866_6867del (ATM) XP_006718906.1:p.Ser2289Ter
XM_006718845.2:c.2822_2823del (ATM) XP_006718908.1:p.Ser941Ter
XM_011542840.3:c.6866_6867del (ATM) XP_011541142.1:p.Ser2289Ter
XM_011542842.3:c.6701_6702del (ATM) XP_011541144.1:p.Ser2234Ter
XM_011542843.2:c.6866_6867del (ATM) XP_011541145.1:p.Ser2289Ter
XM_011542844.3:c.5822_5823del (ATM) XP_011541146.1:p.Ser1941Ter
XM_011542845.2:c.5558_5559del (ATM) XP_011541147.1:p.Ser1853Ter
XM_017017789.2:c.6866_6867del (ATM) XP_016873278.1:p.Ser2289Ter
XM_017017790.2:c.6866_6867del (ATM) XP_016873279.1:p.Ser2289Ter
NM_001330368.2:c.641-17043_641-17042del (C11orf65) NP_001317297.1:n.641-17043_641-17042del
NM_001351110.2:c.*38+9106_*38+9107del (C11orf65) NP_001338039.1:n.*38+9106_*38+9107del
NM_001351834.2:c.6866_6867del (ATM) NP_001338763.1:p.Ser2289Ter
NM_000051.4:c.6866_6867del (ATM) MANE Select NP_000042.3:p.Ser2289Ter