Canonical Allele Identifier: CA1998805487
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108319955_108319958delinsAAAG , CM000673.2:g.108319955_108319958delinsAAAG GRCh38
NC_000011.9:g.108190682_108190685delinsAAAG , CM000673.1:g.108190682_108190685delinsAAAG GRCh37
NC_000011.8:g.107695892_107695895delinsAAAG NCBI36
NG_009830.1:g.102124_102127delinsAAAG , LRG_135:g.102124_102127delinsAAAG
NG_054724.1:g.154875_154878delinsCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.6349_6352delinsAAAG (ATM) ENSP00000388058.2:p.Lys2117=
ENST00000713593.1:c.*5820_*5823delinsAAAG (ATM) ENSP00000518889.1:n.*5820_*5823delinsAAAG
ENST00000278616.9:c.6349_6352delinsAAAG (ATM) ENSP00000278616.4:p.Lys2117=
ENST00000525056.2:n.768_771delinsAAAG (ATM)
ENST00000682286.1:n.1106_1109delinsAAAG (ATM)
ENST00000682302.1:n.767_770delinsAAAG (ATM)
ENST00000683174.1:n.7833_7836delinsAAAG (ATM)
ENST00000683524.1:n.1573_1576delinsAAAG (ATM)
ENST00000684152.1:n.2063_2066delinsAAAG (ATM)
ENST00000527805.6:c.*1413_*1416delinsAAAG (ATM) ENSP00000435747.2:n.*1413_*1416delinsAAAG
ENST00000675595.1:c.*1413_*1416delinsAAAG (ATM) ENSP00000502563.1:n.*1413_*1416delinsAAAG
ENST00000675843.1:c.6349_6352delinsAAAG (ATM) MANE Select ENSP00000501606.1:p.Lys2117=
ENST00000278616.8:c.6349_6352delinsAAAG (ATM) ENSP00000278616.4:p.Lys2117=
ENST00000452508.6:c.6349_6352delinsAAAG (ATM) ENSP00000388058.2:p.Lys2117=
ENST00000524792.5:n.2564_2567delinsAAAG (ATM)
ENST00000525729.5:c.641-10887_641-10884delinsCTTT (C11orf65) ENSP00000433395.1:n.641-10887_641-10884delinsCTTT
ENST00000533690.5:n.1753_1756delinsAAAG (ATM)
NM_000051.3:c.6349_6352delinsAAAG , LRG_135t1:c.6349_6352delinsAAAG (ATM) NP_000042.3:p.Lys2117=
XM_005271561.3:c.6349_6352delinsAAAG (ATM) XP_005271618.2:p.Lys2117=
XM_005271562.3:c.6349_6352delinsAAAG (ATM) XP_005271619.2:p.Lys2117=
XM_006718843.2:c.6349_6352delinsAAAG (ATM) XP_006718906.1:p.Lys2117=
XM_006718845.1:c.2305_2308delinsAAAG (ATM) XP_006718908.1:p.Lys769=
XM_011542840.1:c.6349_6352delinsAAAG (ATM) XP_011541142.1:p.Lys2117=
XM_011542841.1:c.6349_6352delinsAAAG (ATM) XP_011541143.1:p.Lys2117=
XM_011542842.1:c.6184_6187delinsAAAG (ATM) XP_011541144.1:p.Lys2062=
XM_011542843.1:c.6349_6352delinsAAAG (ATM) XP_011541145.1:p.Lys2117=
XM_011542844.1:c.5305_5308delinsAAAG (ATM) XP_011541146.1:p.Lys1769=
XM_011542845.1:c.5041_5044delinsAAAG (ATM) XP_011541147.1:p.Lys1681=
XM_011542847.1:c.1420_1423delinsAAAG (ATM) XP_011541149.1:p.Lys474=
NM_001330368.1:c.641-10887_641-10884delinsCTTT (C11orf65) NP_001317297.1:n.641-10887_641-10884delinsCTTT
NM_001351110.1:c.*39-10887_*39-10884delinsCTTT (C11orf65) NP_001338039.1:n.*39-10887_*39-10884delinsCTTT
NM_001351834.1:c.6349_6352delinsAAAG (ATM) NP_001338763.1:p.Lys2117=
XM_005271562.5:c.6349_6352delinsAAAG (ATM) XP_005271619.2:p.Lys2117=
XM_006718843.4:c.6349_6352delinsAAAG (ATM) XP_006718906.1:p.Lys2117=
XM_006718845.2:c.2305_2308delinsAAAG (ATM) XP_006718908.1:p.Lys769=
XM_011542840.3:c.6349_6352delinsAAAG (ATM) XP_011541142.1:p.Lys2117=
XM_011542842.3:c.6184_6187delinsAAAG (ATM) XP_011541144.1:p.Lys2062=
XM_011542843.2:c.6349_6352delinsAAAG (ATM) XP_011541145.1:p.Lys2117=
XM_011542844.3:c.5305_5308delinsAAAG (ATM) XP_011541146.1:p.Lys1769=
XM_011542845.2:c.5041_5044delinsAAAG (ATM) XP_011541147.1:p.Lys1681=
XM_017017789.2:c.6349_6352delinsAAAG (ATM) XP_016873278.1:p.Lys2117=
XM_017017790.2:c.6349_6352delinsAAAG (ATM) XP_016873279.1:p.Lys2117=
XM_017017791.1:c.6349_6352delinsAAAG (ATM) XP_016873280.1:p.Lys2117=
NM_001330368.2:c.641-10887_641-10884delinsCTTT (C11orf65) NP_001317297.1:n.641-10887_641-10884delinsCTTT
NM_001351110.2:c.*39-10887_*39-10884delinsCTTT (C11orf65) NP_001338039.1:n.*39-10887_*39-10884delinsCTTT
NM_001351834.2:c.6349_6352delinsAAAG (ATM) NP_001338763.1:p.Lys2117=
NM_000051.4:c.6349_6352delinsAAAG (ATM) MANE Select NP_000042.3:p.Lys2117=