Canonical Allele Identifier: CA2695215476
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108326160_108326161delinsTG , CM000673.2:g.108326160_108326161delinsTG GRCh38
NC_000011.9:g.108196887_108196888delinsTG , CM000673.1:g.108196887_108196888delinsTG GRCh37
NC_000011.8:g.107702097_107702098delinsTG NCBI36
NG_009830.1:g.108329_108330delinsTG , LRG_135:g.108329_108330delinsTG
NG_054724.1:g.148672_148673delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.6910_6911delinsTG (ATM) ENSP00000388058.2:p.Glu2304Trp
ENST00000713593.1:c.*6381_*6382delinsTG (ATM) ENSP00000518889.1:n.*6381_*6382delinsTG
ENST00000278616.9:c.6910_6911delinsTG (ATM) ENSP00000278616.4:p.Glu2304Trp
ENST00000525056.2:n.1329_1330delinsTG (ATM)
ENST00000682286.1:n.1667_1668delinsTG (ATM)
ENST00000682302.1:n.1328_1329delinsTG (ATM)
ENST00000683174.1:n.8394_8395delinsTG (ATM)
ENST00000683524.1:n.2134_2135delinsTG (ATM)
ENST00000684152.1:n.2624_2625delinsTG (ATM)
ENST00000527805.6:c.*1974_*1975delinsTG (ATM) ENSP00000435747.2:n.*1974_*1975delinsTG
ENST00000675595.1:c.*2045_*2046delinsTG (ATM) ENSP00000502563.1:n.*2045_*2046delinsTG
ENST00000675843.1:c.6910_6911delinsTG (ATM) MANE Select ENSP00000501606.1:p.Glu2304Trp
ENST00000278616.8:c.6910_6911delinsTG (ATM) ENSP00000278616.4:p.Glu2304Trp
ENST00000452508.6:c.6910_6911delinsTG (ATM) ENSP00000388058.2:p.Glu2304Trp
ENST00000524792.5:n.3125_3126delinsTG (ATM)
ENST00000525729.5:c.641-17090_641-17089delinsCA (C11orf65) ENSP00000433395.1:n.641-17090_641-17089delinsCA
ENST00000533690.5:n.2314_2315delinsTG (ATM)
NM_000051.3:c.6910_6911delinsTG , LRG_135t1:c.6910_6911delinsTG (ATM) NP_000042.3:p.Glu2304Trp
XM_005271561.3:c.6910_6911delinsTG (ATM) XP_005271618.2:p.Glu2304Trp
XM_005271562.3:c.6910_6911delinsTG (ATM) XP_005271619.2:p.Glu2304Trp
XM_006718843.2:c.6910_6911delinsTG (ATM) XP_006718906.1:p.Glu2304Trp
XM_006718845.1:c.2866_2867delinsTG (ATM) XP_006718908.1:p.Glu956Trp
XM_011542840.1:c.6910_6911delinsTG (ATM) XP_011541142.1:p.Glu2304Trp
XM_011542841.1:c.6910_6911delinsTG (ATM) XP_011541143.1:p.Glu2304Trp
XM_011542842.1:c.6745_6746delinsTG (ATM) XP_011541144.1:p.Glu2249Trp
XM_011542843.1:c.6910_6911delinsTG (ATM) XP_011541145.1:p.Glu2304Trp
XM_011542844.1:c.5866_5867delinsTG (ATM) XP_011541146.1:p.Glu1956Trp
XM_011542845.1:c.5602_5603delinsTG (ATM) XP_011541147.1:p.Glu1868Trp
XM_011542847.1:c.1981_1982delinsTG (ATM) XP_011541149.1:p.Glu661Trp
NM_001330368.1:c.641-17090_641-17089delinsCA (C11orf65) NP_001317297.1:n.641-17090_641-17089delinsCA
NM_001351110.1:c.*38+9059_*38+9060delinsCA (C11orf65) NP_001338039.1:n.*38+9059_*38+9060delinsCA
NM_001351834.1:c.6910_6911delinsTG (ATM) NP_001338763.1:p.Glu2304Trp
XM_005271562.5:c.6910_6911delinsTG (ATM) XP_005271619.2:p.Glu2304Trp
XM_006718843.4:c.6910_6911delinsTG (ATM) XP_006718906.1:p.Glu2304Trp
XM_006718845.2:c.2866_2867delinsTG (ATM) XP_006718908.1:p.Glu956Trp
XM_011542840.3:c.6910_6911delinsTG (ATM) XP_011541142.1:p.Glu2304Trp
XM_011542842.3:c.6745_6746delinsTG (ATM) XP_011541144.1:p.Glu2249Trp
XM_011542843.2:c.6910_6911delinsTG (ATM) XP_011541145.1:p.Glu2304Trp
XM_011542844.3:c.5866_5867delinsTG (ATM) XP_011541146.1:p.Glu1956Trp
XM_011542845.2:c.5602_5603delinsTG (ATM) XP_011541147.1:p.Glu1868Trp
XM_017017789.2:c.6910_6911delinsTG (ATM) XP_016873278.1:p.Glu2304Trp
XM_017017790.2:c.6910_6911delinsTG (ATM) XP_016873279.1:p.Glu2304Trp
NM_001330368.2:c.641-17090_641-17089delinsCA (C11orf65) NP_001317297.1:n.641-17090_641-17089delinsCA
NM_001351110.2:c.*38+9059_*38+9060delinsCA (C11orf65) NP_001338039.1:n.*38+9059_*38+9060delinsCA
NM_001351834.2:c.6910_6911delinsTG (ATM) NP_001338763.1:p.Glu2304Trp
NM_000051.4:c.6910_6911delinsTG (ATM) MANE Select NP_000042.3:p.Glu2304Trp