Canonical Allele Identifier: CA382516753
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108343358A>T , CM000673.2:g.108343358A>T GRCh38
NC_000011.9:g.108214085A>T , CM000673.1:g.108214085A>T GRCh37
NC_000011.8:g.107719295A>T NCBI36
NG_009830.1:g.125527A>T , LRG_135:g.125527A>T
NG_054724.1:g.131475T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.8405A>T (ATM) ENSP00000388058.2:p.Gln2802Leu
ENST00000713593.1:c.*7876A>T (ATM) ENSP00000518889.1:n.*7876A>T
ENST00000278616.9:c.8405A>T (ATM) ENSP00000278616.4:p.Gln2802Leu
ENST00000638786.2:n.1103A>T (ATM)
ENST00000682286.1:n.3162A>T (ATM)
ENST00000682302.1:n.2823A>T (ATM)
ENST00000683174.1:n.9889A>T (ATM)
ENST00000683524.1:n.3629A>T (ATM)
ENST00000684152.1:n.3821A>T (ATM)
ENST00000684180.1:n.879A>T (ATM)
ENST00000684447.1:n.4898A>T (ATM)
ENST00000527805.6:c.*3469A>T (ATM) ENSP00000435747.2:n.*3469A>T
ENST00000675595.1:c.*3540A>T (ATM) ENSP00000502563.1:n.*3540A>T
ENST00000675843.1:c.8405A>T (ATM) MANE Select ENSP00000501606.1:p.Gln2802Leu
ENST00000278616.8:c.8405A>T (ATM) ENSP00000278616.4:p.Gln2802Leu
ENST00000452508.6:c.8405A>T (ATM) ENSP00000388058.2:p.Gln2802Leu
ENST00000524755.5:c.227-8066T>A (C11orf65)
ENST00000524792.5:n.4620A>T (ATM)
ENST00000525729.5:c.641-34287T>A (C11orf65) ENSP00000433395.1:n.641-34287T>A
ENST00000526725.1:n.272-2994T>A (C11orf65)
ENST00000527531.5:c.*1197-8066T>A (C11orf65) ENSP00000431706.1:n.*1197-8066T>A
ENST00000615746.4:c.*1197-8066T>A (C11orf65) ENSP00000483537.1:n.*1197-8066T>A
NM_000051.3:c.8405A>T , LRG_135t1:c.8405A>T (ATM) NP_000042.3:p.Gln2802Leu
XM_005271414.3:c.788-8066T>A (C11orf65) XP_005271471.1:n.788-8066T>A
XM_005271415.3:c.732-8066T>A (C11orf65) XP_005271472.1:n.732-8066T>A
XM_005271561.3:c.8405A>T (ATM) XP_005271618.2:p.Gln2802Leu
XM_005271562.3:c.8405A>T (ATM) XP_005271619.2:p.Gln2802Leu
XM_006718843.2:c.8405A>T (ATM) XP_006718906.1:p.Gln2802Leu
XM_006718845.1:c.4361A>T (ATM) XP_006718908.1:p.Gln1454Leu
XM_011542640.1:c.788-2994T>A (C11orf65) XP_011540942.1:n.788-2994T>A
XM_011542643.1:c.732-2994T>A (C11orf65) XP_011540945.1:n.732-2994T>A
XM_011542840.1:c.8405A>T (ATM) XP_011541142.1:p.Gln2802Leu
XM_011542841.1:c.8405A>T (ATM) XP_011541143.1:p.Gln2802Leu
XM_011542842.1:c.8240A>T (ATM) XP_011541144.1:p.Gln2747Leu
XM_011542843.1:c.8405A>T (ATM) XP_011541145.1:p.Gln2802Leu
XM_011542844.1:c.7361A>T (ATM) XP_011541146.1:p.Gln2454Leu
XM_011542845.1:c.7097A>T (ATM) XP_011541147.1:p.Gln2366Leu
XM_011542847.1:c.3476A>T (ATM) XP_011541149.1:p.Gln1159Leu
NM_001330368.1:c.641-34287T>A (C11orf65) NP_001317297.1:n.641-34287T>A
NM_001351110.1:c.695-8066T>A (C11orf65) NP_001338039.1:n.695-8066T>A
NM_001351834.1:c.8405A>T (ATM) NP_001338763.1:p.Gln2802Leu
NR_147053.2:n.2302-8066T>A (C11orf65)
XM_005271414.4:c.788-8066T>A (C11orf65) XP_005271471.1:n.788-8066T>A
XM_005271415.4:c.732-8066T>A (C11orf65) XP_005271472.1:n.732-8066T>A
XM_005271562.5:c.8405A>T (ATM) XP_005271619.2:p.Gln2802Leu
XM_006718843.4:c.8405A>T (ATM) XP_006718906.1:p.Gln2802Leu
XM_006718845.2:c.4361A>T (ATM) XP_006718908.1:p.Gln1454Leu
XM_011542640.2:c.788-2994T>A (C11orf65) XP_011540942.1:n.788-2994T>A
XM_011542643.2:c.732-2994T>A (C11orf65) XP_011540945.1:n.732-2994T>A
XM_011542840.3:c.8405A>T (ATM) XP_011541142.1:p.Gln2802Leu
XM_011542842.3:c.8240A>T (ATM) XP_011541144.1:p.Gln2747Leu
XM_011542843.2:c.8405A>T (ATM) XP_011541145.1:p.Gln2802Leu
XM_011542844.3:c.7361A>T (ATM) XP_011541146.1:p.Gln2454Leu
XM_011542845.2:c.7097A>T (ATM) XP_011541147.1:p.Gln2366Leu
XM_017017247.1:c.904-2994T>A (C11orf65) XP_016872736.1:n.904-2994T>A
XM_017017789.2:c.8405A>T (ATM) XP_016873278.1:p.Gln2802Leu
XM_017017790.2:c.8405A>T (ATM) XP_016873279.1:p.Gln2802Leu
NM_001330368.2:c.641-34287T>A (C11orf65) NP_001317297.1:n.641-34287T>A
NM_001351110.2:c.695-8066T>A (C11orf65) NP_001338039.1:n.695-8066T>A
NM_001351834.2:c.8405A>T (ATM) NP_001338763.1:p.Gln2802Leu
NM_000051.4:c.8405A>T (ATM) MANE Select NP_000042.3:p.Gln2802Leu
NR_147053.3:n.2300-8066T>A (C11orf65)