Canonical Allele Identifier: CA1998810319
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108331896A= , CM000673.2:g.108331896A= GRCh38
NC_000011.9:g.108202623A= , CM000673.1:g.108202623A= GRCh37
NC_000011.8:g.107707833A= NCBI36
NG_009830.1:g.114065A= , LRG_135:g.114065A=
NG_054724.1:g.142937T=

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.7647A= (ATM) ENSP00000388058.2:p.Ser2549=
ENST00000713593.1:c.*7118A= (ATM) ENSP00000518889.1:n.*7118A=
ENST00000278616.9:c.7647A= (ATM) ENSP00000278616.4:p.Ser2549=
ENST00000525056.2:n.2066A= (ATM)
ENST00000525537.3:n.604A= (ATM)
ENST00000638786.2:n.484A= (ATM)
ENST00000682286.1:n.2404A= (ATM)
ENST00000682302.1:n.2065A= (ATM)
ENST00000683174.1:n.9131A= (ATM)
ENST00000683524.1:n.2871A= (ATM)
ENST00000684152.1:n.3343+339A= (ATM)
ENST00000684447.1:n.2431A= (ATM)
ENST00000527805.6:c.*2711A= (ATM) ENSP00000435747.2:n.*2711A=
ENST00000675595.1:c.*2782A= (ATM) ENSP00000502563.1:n.*2782A=
ENST00000675843.1:c.7647A= (ATM) MANE Select ENSP00000501606.1:p.Ser2549=
ENST00000278616.8:c.7647A= (ATM) ENSP00000278616.4:p.Ser2549=
ENST00000452508.6:c.7647A= (ATM) ENSP00000388058.2:p.Ser2549=
ENST00000524755.5:c.300-329T= (C11orf65)
ENST00000524792.5:n.3862A= (ATM)
ENST00000525729.5:c.641-22825T= (C11orf65) ENSP00000433395.1:n.641-22825T=
ENST00000527531.5:c.*1270-329T= (C11orf65) ENSP00000431706.1:n.*1270-329T=
ENST00000533690.5:n.3051A= (ATM)
ENST00000615746.4:c.*1270-329T= (C11orf65) ENSP00000483537.1:n.*1270-329T=
NM_000051.3:c.7647A= , LRG_135t1:c.7647A= (ATM) NP_000042.3:p.Ser2549=
XM_005271414.3:c.*39-329T= (C11orf65) XP_005271471.1:n.*39-329T=
XM_005271415.3:c.805-329T= (C11orf65) XP_005271472.1:n.805-329T=
XM_005271561.3:c.7647A= (ATM) XP_005271618.2:p.Ser2549=
XM_005271562.3:c.7647A= (ATM) XP_005271619.2:p.Ser2549=
XM_006718843.2:c.7647A= (ATM) XP_006718906.1:p.Ser2549=
XM_006718845.1:c.3603A= (ATM) XP_006718908.1:p.Ser1201=
XM_011542840.1:c.7647A= (ATM) XP_011541142.1:p.Ser2549=
XM_011542841.1:c.7647A= (ATM) XP_011541143.1:p.Ser2549=
XM_011542842.1:c.7482A= (ATM) XP_011541144.1:p.Ser2494=
XM_011542843.1:c.7647A= (ATM) XP_011541145.1:p.Ser2549=
XM_011542844.1:c.6603A= (ATM) XP_011541146.1:p.Ser2201=
XM_011542845.1:c.6339A= (ATM) XP_011541147.1:p.Ser2113=
XM_011542847.1:c.2718A= (ATM) XP_011541149.1:p.Ser906=
NM_001330368.1:c.641-22825T= (C11orf65) NP_001317297.1:n.641-22825T=
NM_001351110.1:c.*38+3324T= (C11orf65) NP_001338039.1:n.*38+3324T=
NM_001351834.1:c.7647A= (ATM) NP_001338763.1:p.Ser2549=
NR_147053.2:n.2375-329T= (C11orf65)
XM_005271414.4:c.*39-329T= (C11orf65) XP_005271471.1:n.*39-329T=
XM_005271415.4:c.805-329T= (C11orf65) XP_005271472.1:n.805-329T=
XM_005271562.5:c.7647A= (ATM) XP_005271619.2:p.Ser2549=
XM_006718843.4:c.7647A= (ATM) XP_006718906.1:p.Ser2549=
XM_006718845.2:c.3603A= (ATM) XP_006718908.1:p.Ser1201=
XM_011542840.3:c.7647A= (ATM) XP_011541142.1:p.Ser2549=
XM_011542842.3:c.7482A= (ATM) XP_011541144.1:p.Ser2494=
XM_011542843.2:c.7647A= (ATM) XP_011541145.1:p.Ser2549=
XM_011542844.3:c.6603A= (ATM) XP_011541146.1:p.Ser2201=
XM_011542845.2:c.6339A= (ATM) XP_011541147.1:p.Ser2113=
XM_017017789.2:c.7647A= (ATM) XP_016873278.1:p.Ser2549=
XM_017017790.2:c.7647A= (ATM) XP_016873279.1:p.Ser2549=
NM_001330368.2:c.641-22825T= (C11orf65) NP_001317297.1:n.641-22825T=
NM_001351110.2:c.*38+3324T= (C11orf65) NP_001338039.1:n.*38+3324T=
NM_001351834.2:c.7647A= (ATM) NP_001338763.1:p.Ser2549=
NM_000051.4:c.7647A= (ATM) MANE Select NP_000042.3:p.Ser2549=
NR_147053.3:n.2373-329T= (C11orf65)