Canonical Allele Identifier: CA1998817813
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108347278G= , CM000673.2:g.108347278G= GRCh38
NC_000011.9:g.108218005G= , CM000673.1:g.108218005G= GRCh37
NC_000011.8:g.107723215G= NCBI36
NG_009830.1:g.129447G= , LRG_135:g.129447G=
NG_054724.1:g.127555C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.8585-1G= (ATM) ENSP00000388058.2:n.8585-1G=
ENST00000713593.1:c.*8056-1G= (ATM) ENSP00000518889.1:n.*8056-1G=
ENST00000278616.9:c.8585-1G= (ATM) ENSP00000278616.4:n.8585-1G=
ENST00000638786.2:n.1283-1G= (ATM)
ENST00000682286.1:n.3342-1G= (ATM)
ENST00000682302.1:n.3003-1G= (ATM)
ENST00000683174.1:n.10069-1G= (ATM)
ENST00000683524.1:n.3809-1G= (ATM)
ENST00000684152.1:n.4001-1G= (ATM)
ENST00000684180.1:n.1059-1G= (ATM)
ENST00000684447.1:n.5078-1G= (ATM)
ENST00000527805.6:c.*3649-1G= (ATM) ENSP00000435747.2:n.*3649-1G=
ENST00000675595.1:c.*3720-1G= (ATM) ENSP00000502563.1:n.*3720-1G=
ENST00000675843.1:c.8585-1G= (ATM) MANE Select ENSP00000501606.1:n.8585-1G=
ENST00000278616.8:c.8585-1G= (ATM) ENSP00000278616.4:n.8585-1G=
ENST00000452508.6:c.8585-1G= (ATM) ENSP00000388058.2:n.8585-1G=
ENST00000524755.5:c.227-11986C= (C11orf65)
ENST00000524792.5:n.4800-1G= (ATM)
ENST00000525178.5:n.73-1G= (ATM)
ENST00000525729.5:c.641-38207C= (C11orf65) ENSP00000433395.1:n.641-38207C=
ENST00000526725.1:n.272-6914C= (C11orf65)
ENST00000527531.5:c.*1196+7637C= (C11orf65) ENSP00000431706.1:n.*1196+7637C=
ENST00000615746.4:c.*1196+7637C= (C11orf65) ENSP00000483537.1:n.*1196+7637C=
NM_000051.3:c.8585-1G= , LRG_135t1:c.8585-1G= (ATM) NP_000042.3:n.8585-1G=
XM_005271414.3:c.788-11986C= (C11orf65) XP_005271471.1:n.788-11986C=
XM_005271415.3:c.732-11986C= (C11orf65) XP_005271472.1:n.732-11986C=
XM_005271561.3:c.8585-1G= (ATM) XP_005271618.2:n.8585-1G=
XM_005271562.3:c.8585-1G= (ATM) XP_005271619.2:n.8585-1G=
XM_006718843.2:c.8585-1G= (ATM) XP_006718906.1:n.8585-1G=
XM_006718845.1:c.4541-1G= (ATM) XP_006718908.1:n.4541-1G=
XM_011542640.1:c.788-6914C= (C11orf65) XP_011540942.1:n.788-6914C=
XM_011542643.1:c.732-6914C= (C11orf65) XP_011540945.1:n.732-6914C=
XM_011542840.1:c.8585-1G= (ATM) XP_011541142.1:n.8585-1G=
XM_011542841.1:c.8585-1G= (ATM) XP_011541143.1:n.8585-1G=
XM_011542842.1:c.8420-1G= (ATM) XP_011541144.1:n.8420-1G=
XM_011542843.1:c.8585-1G= (ATM) XP_011541145.1:n.8585-1G=
XM_011542844.1:c.7541-1G= (ATM) XP_011541146.1:n.7541-1G=
XM_011542845.1:c.7277-1G= (ATM) XP_011541147.1:n.7277-1G=
XM_011542847.1:c.3656-1G= (ATM) XP_011541149.1:n.3656-1G=
NM_001330368.1:c.641-38207C= (C11orf65) NP_001317297.1:n.641-38207C=
NM_001351110.1:c.695-11986C= (C11orf65) NP_001338039.1:n.695-11986C=
NM_001351834.1:c.8585-1G= (ATM) NP_001338763.1:n.8585-1G=
NR_147053.2:n.2301+7637C= (C11orf65)
XM_005271414.4:c.788-11986C= (C11orf65) XP_005271471.1:n.788-11986C=
XM_005271415.4:c.732-11986C= (C11orf65) XP_005271472.1:n.732-11986C=
XM_005271562.5:c.8585-1G= (ATM) XP_005271619.2:n.8585-1G=
XM_006718843.4:c.8585-1G= (ATM) XP_006718906.1:n.8585-1G=
XM_006718845.2:c.4541-1G= (ATM) XP_006718908.1:n.4541-1G=
XM_011542640.2:c.788-6914C= (C11orf65) XP_011540942.1:n.788-6914C=
XM_011542643.2:c.732-6914C= (C11orf65) XP_011540945.1:n.732-6914C=
XM_011542840.3:c.8585-1G= (ATM) XP_011541142.1:n.8585-1G=
XM_011542842.3:c.8420-1G= (ATM) XP_011541144.1:n.8420-1G=
XM_011542843.2:c.8585-1G= (ATM) XP_011541145.1:n.8585-1G=
XM_011542844.3:c.7541-1G= (ATM) XP_011541146.1:n.7541-1G=
XM_011542845.2:c.7277-1G= (ATM) XP_011541147.1:n.7277-1G=
XM_017017247.1:c.904-6914C= (C11orf65) XP_016872736.1:n.904-6914C=
XM_017017789.2:c.8585-1G= (ATM) XP_016873278.1:n.8585-1G=
XM_017017790.2:c.8585-1G= (ATM) XP_016873279.1:n.8585-1G=
NM_001330368.2:c.641-38207C= (C11orf65) NP_001317297.1:n.641-38207C=
NM_001351110.2:c.695-11986C= (C11orf65) NP_001338039.1:n.695-11986C=
NM_001351834.2:c.8585-1G= (ATM) NP_001338763.1:n.8585-1G=
NM_000051.4:c.8585-1G= (ATM) MANE Select NP_000042.3:n.8585-1G=
NR_147053.3:n.2299+7637C= (C11orf65)