Canonical Allele Identifier: CA2615863451
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108335879_108335882del , CM000673.2:g.108335879_108335882del GRCh38
NC_000011.9:g.108206606_108206609del , CM000673.1:g.108206606_108206609del GRCh37
NC_000011.8:g.107711816_107711819del NCBI36
NG_009830.1:g.118048_118051del , LRG_135:g.118048_118051del
NG_054724.1:g.138951_138954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.8186_8189del (ATM) ENSP00000388058.2:p.Gln2729ArgfsTer21
ENST00000713593.1:c.*7657_*7660del (ATM) ENSP00000518889.1:n.*7657_*7660del
ENST00000278616.9:c.8186_8189del (ATM) ENSP00000278616.4:p.Gln2729ArgfsTer21
ENST00000525056.2:n.2605_2608del (ATM)
ENST00000638786.2:n.884_887del (ATM)
ENST00000682286.1:n.2943_2946del (ATM)
ENST00000682302.1:n.2604_2607del (ATM)
ENST00000683174.1:n.9670_9673del (ATM)
ENST00000683524.1:n.3410_3413del (ATM)
ENST00000684152.1:n.3602_3605del (ATM)
ENST00000684180.1:n.660_663del (ATM)
ENST00000684447.1:n.4679_4682del (ATM)
ENST00000527805.6:c.*3250_*3253del (ATM) ENSP00000435747.2:n.*3250_*3253del
ENST00000675595.1:c.*3321_*3324del (ATM) ENSP00000502563.1:n.*3321_*3324del
ENST00000675843.1:c.8186_8189del (ATM) MANE Select ENSP00000501606.1:p.Gln2729ArgfsTer21
ENST00000278616.8:c.8186_8189del (ATM) ENSP00000278616.4:p.Gln2729ArgfsTer21
ENST00000452508.6:c.8186_8189del (ATM) ENSP00000388058.2:p.Gln2729ArgfsTer21
ENST00000524755.5:c.227-590_227-587del (C11orf65)
ENST00000524792.5:n.4401_4404del (ATM)
ENST00000525056.1:n.383_386del (ATM)
ENST00000525729.5:c.641-26811_641-26808del (C11orf65) ENSP00000433395.1:n.641-26811_641-26808del
ENST00000527531.5:c.*1197-590_*1197-587del (C11orf65) ENSP00000431706.1:n.*1197-590_*1197-587del
ENST00000533979.5:n.398_401del (ATM)
ENST00000615746.4:c.*1197-590_*1197-587del (C11orf65) ENSP00000483537.1:n.*1197-590_*1197-587del
NM_000051.3:c.8186_8189del , LRG_135t1:c.8186_8189del (ATM) NP_000042.3:p.Gln2729ArgfsTer21
XM_005271414.3:c.788-590_788-587del (C11orf65) XP_005271471.1:n.788-590_788-587del
XM_005271415.3:c.732-590_732-587del (C11orf65) XP_005271472.1:n.732-590_732-587del
XM_005271561.3:c.8186_8189del (ATM) XP_005271618.2:p.Gln2729ArgfsTer21
XM_005271562.3:c.8186_8189del (ATM) XP_005271619.2:p.Gln2729ArgfsTer21
XM_006718843.2:c.8186_8189del (ATM) XP_006718906.1:p.Gln2729ArgfsTer21
XM_006718845.1:c.4142_4145del (ATM) XP_006718908.1:p.Gln1381ArgfsTer21
XM_011542840.1:c.8186_8189del (ATM) XP_011541142.1:p.Gln2729ArgfsTer21
XM_011542841.1:c.8186_8189del (ATM) XP_011541143.1:p.Gln2729ArgfsTer21
XM_011542842.1:c.8021_8024del (ATM) XP_011541144.1:p.Gln2674ArgfsTer21
XM_011542843.1:c.8186_8189del (ATM) XP_011541145.1:p.Gln2729ArgfsTer21
XM_011542844.1:c.7142_7145del (ATM) XP_011541146.1:p.Gln2381ArgfsTer21
XM_011542845.1:c.6878_6881del (ATM) XP_011541147.1:p.Gln2293ArgfsTer21
XM_011542847.1:c.3257_3260del (ATM) XP_011541149.1:p.Gln1086ArgfsTer21
NM_001330368.1:c.641-26811_641-26808del (C11orf65) NP_001317297.1:n.641-26811_641-26808del
NM_001351110.1:c.695-590_695-587del (C11orf65) NP_001338039.1:n.695-590_695-587del
NM_001351834.1:c.8186_8189del (ATM) NP_001338763.1:p.Gln2729ArgfsTer21
NR_147053.2:n.2302-590_2302-587del (C11orf65)
XM_005271414.4:c.788-590_788-587del (C11orf65) XP_005271471.1:n.788-590_788-587del
XM_005271415.4:c.732-590_732-587del (C11orf65) XP_005271472.1:n.732-590_732-587del
XM_005271562.5:c.8186_8189del (ATM) XP_005271619.2:p.Gln2729ArgfsTer21
XM_006718843.4:c.8186_8189del (ATM) XP_006718906.1:p.Gln2729ArgfsTer21
XM_006718845.2:c.4142_4145del (ATM) XP_006718908.1:p.Gln1381ArgfsTer21
XM_011542840.3:c.8186_8189del (ATM) XP_011541142.1:p.Gln2729ArgfsTer21
XM_011542842.3:c.8021_8024del (ATM) XP_011541144.1:p.Gln2674ArgfsTer21
XM_011542843.2:c.8186_8189del (ATM) XP_011541145.1:p.Gln2729ArgfsTer21
XM_011542844.3:c.7142_7145del (ATM) XP_011541146.1:p.Gln2381ArgfsTer21
XM_011542845.2:c.6878_6881del (ATM) XP_011541147.1:p.Gln2293ArgfsTer21
XM_017017789.2:c.8186_8189del (ATM) XP_016873278.1:p.Gln2729ArgfsTer21
XM_017017790.2:c.8186_8189del (ATM) XP_016873279.1:p.Gln2729ArgfsTer21
NM_001330368.2:c.641-26811_641-26808del (C11orf65) NP_001317297.1:n.641-26811_641-26808del
NM_001351110.2:c.695-590_695-587del (C11orf65) NP_001338039.1:n.695-590_695-587del
NM_001351834.2:c.8186_8189del (ATM) NP_001338763.1:p.Gln2729ArgfsTer21
NM_000051.4:c.8186_8189del (ATM) MANE Select NP_000042.3:p.Gln2729ArgfsTer21
NR_147053.3:n.2300-590_2300-587del (C11orf65)