Canonical Allele Identifier: CA3186315522
Community Standard Title: NM_000051.4(ATM):c.8533T= (p.Trp2845=)
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108345857T= , CM000673.2:g.108345857T= GRCh38
NC_000011.9:g.108216584T= , CM000673.1:g.108216584T= GRCh37
NC_000011.8:g.107721794T= NCBI36
NG_009830.1:g.128026T= , LRG_135:g.128026T=
NG_054724.1:g.128976A=

Transcript Alleles

HGVS Amino-acid Change
NM_000051.4:c.8533T= (ATM) MANE Select NP_000042.3:p.Trp2845=
ENST00000675843.1:c.8533T= (ATM) MANE Select ENSP00000501606.1:p.Trp2845=
NM_000051.3:c.8533T= , LRG_135t1:c.8533T= (ATM) NP_000042.3:p.Trp2845=
NM_001330368.1:c.641-36786A= (C11orf65) NP_001317297.1:n.641-36786A=
NM_001330368.2:c.641-36786A= (C11orf65) NP_001317297.1:n.641-36786A=
NM_001351110.1:c.695-10565A= (C11orf65) NP_001338039.1:n.695-10565A=
NM_001351110.2:c.695-10565A= (C11orf65) NP_001338039.1:n.695-10565A=
NM_001351834.1:c.8533T= (ATM) NP_001338763.1:p.Trp2845=
NM_001351834.2:c.8533T= (ATM) NP_001338763.1:p.Trp2845=
NR_147053.2:n.2301+9058A= (C11orf65)
NR_147053.3:n.2299+9058A= (C11orf65)
ENST00000278616.8:c.8533T= (ATM) ENSP00000278616.4:p.Trp2845=
ENST00000278616.9:c.8533T= (ATM) ENSP00000278616.4:p.Trp2845=
ENST00000452508.6:c.8533T= (ATM) ENSP00000388058.2:p.Trp2845=
ENST00000452508.7:c.8533T= (ATM) ENSP00000388058.2:p.Trp2845=
ENST00000524755.5:c.227-10565A= (C11orf65)
ENST00000524792.5:n.4748T= (ATM)
ENST00000525729.5:c.641-36786A= (C11orf65) ENSP00000433395.1:n.641-36786A=
ENST00000526725.1:n.272-5493A= (C11orf65)
ENST00000527531.5:c.*1196+9058A= (C11orf65) ENSP00000431706.1:n.*1196+9058A=
ENST00000527805.6:c.*3597T= (ATM) ENSP00000435747.2:n.*3597T=
ENST00000615746.4:c.*1196+9058A= (C11orf65) ENSP00000483537.1:n.*1196+9058A=
ENST00000638786.2:n.1231T= (ATM)
ENST00000675595.1:c.*3668T= (ATM) ENSP00000502563.1:n.*3668T=
ENST00000682286.1:n.3290T= (ATM)
ENST00000682302.1:n.2951T= (ATM)
ENST00000683174.1:n.10017T= (ATM)
ENST00000683524.1:n.3757T= (ATM)
ENST00000684152.1:n.3949T= (ATM)
ENST00000684180.1:n.1007T= (ATM)
ENST00000684447.1:n.5026T= (ATM)
ENST00000713593.1:c.*8004T= (ATM) ENSP00000518889.1:n.*8004T=
XM_005271414.3:c.788-10565A= (C11orf65) XP_005271471.1:n.788-10565A=
XM_005271414.4:c.788-10565A= (C11orf65) XP_005271471.1:n.788-10565A=
XM_005271415.3:c.732-10565A= (C11orf65) XP_005271472.1:n.732-10565A=
XM_005271415.4:c.732-10565A= (C11orf65) XP_005271472.1:n.732-10565A=
XM_005271561.3:c.8533T= (ATM) XP_005271618.2:p.Trp2845=
XM_005271562.3:c.8533T= (ATM) XP_005271619.2:p.Trp2845=
XM_005271562.5:c.8533T= (ATM) XP_005271619.2:p.Trp2845=
XM_006718843.2:c.8533T= (ATM) XP_006718906.1:p.Trp2845=
XM_006718843.4:c.8533T= (ATM) XP_006718906.1:p.Trp2845=
XM_006718845.1:c.4489T= (ATM) XP_006718908.1:p.Trp1497=
XM_006718845.2:c.4489T= (ATM) XP_006718908.1:p.Trp1497=
XM_011542640.1:c.788-5493A= (C11orf65) XP_011540942.1:n.788-5493A=
XM_011542640.2:c.788-5493A= (C11orf65) XP_011540942.1:n.788-5493A=
XM_011542643.1:c.732-5493A= (C11orf65) XP_011540945.1:n.732-5493A=
XM_011542643.2:c.732-5493A= (C11orf65) XP_011540945.1:n.732-5493A=
XM_011542840.1:c.8533T= (ATM) XP_011541142.1:p.Trp2845=
XM_011542840.3:c.8533T= (ATM) XP_011541142.1:p.Trp2845=
XM_011542841.1:c.8533T= (ATM) XP_011541143.1:p.Trp2845=
XM_011542842.1:c.8368T= (ATM) XP_011541144.1:p.Trp2790=
XM_011542842.3:c.8368T= (ATM) XP_011541144.1:p.Trp2790=
XM_011542843.1:c.8533T= (ATM) XP_011541145.1:p.Trp2845=
XM_011542843.2:c.8533T= (ATM) XP_011541145.1:p.Trp2845=
XM_011542844.1:c.7489T= (ATM) XP_011541146.1:p.Trp2497=
XM_011542844.3:c.7489T= (ATM) XP_011541146.1:p.Trp2497=
XM_011542845.1:c.7225T= (ATM) XP_011541147.1:p.Trp2409=
XM_011542845.2:c.7225T= (ATM) XP_011541147.1:p.Trp2409=
XM_011542847.1:c.3604T= (ATM) XP_011541149.1:p.Trp1202=
XM_017017247.1:c.904-5493A= (C11orf65) XP_016872736.1:n.904-5493A=
XM_017017789.2:c.8533T= (ATM) XP_016873278.1:p.Trp2845=
XM_017017790.2:c.8533T= (ATM) XP_016873279.1:p.Trp2845=