Canonical Allele Identifier: CA601727571
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108335853_108335855dup , CM000673.2:g.108335853_108335855dup GRCh38
NC_000011.9:g.108206580_108206582dup , CM000673.1:g.108206580_108206582dup GRCh37
NC_000011.8:g.107711790_107711792dup NCBI36
NG_009830.1:g.118022_118024dup , LRG_135:g.118022_118024dup
NG_054724.1:g.138981_138983dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.8160_8162dup (ATM) ENSP00000388058.2:p.Asp2721_Leu2722insAsp
ENST00000713593.1:c.*7631_*7633dup (ATM) ENSP00000518889.1:n.*7631_*7633dup
ENST00000278616.9:c.8160_8162dup (ATM) ENSP00000278616.4:p.Asp2721_Leu2722insAsp
ENST00000525056.2:n.2579_2581dup (ATM)
ENST00000638786.2:n.858_860dup (ATM)
ENST00000682286.1:n.2917_2919dup (ATM)
ENST00000682302.1:n.2578_2580dup (ATM)
ENST00000683174.1:n.9644_9646dup (ATM)
ENST00000683524.1:n.3384_3386dup (ATM)
ENST00000684152.1:n.3576_3578dup (ATM)
ENST00000684180.1:n.634_636dup (ATM)
ENST00000684447.1:n.4653_4655dup (ATM)
ENST00000527805.6:c.*3224_*3226dup (ATM) ENSP00000435747.2:n.*3224_*3226dup
ENST00000675595.1:c.*3295_*3297dup (ATM) ENSP00000502563.1:n.*3295_*3297dup
ENST00000675843.1:c.8160_8162dup (ATM) MANE Select ENSP00000501606.1:p.Asp2721_Leu2722insAsp
ENST00000278616.8:c.8160_8162dup (ATM) ENSP00000278616.4:p.Asp2721_Leu2722insAsp
ENST00000452508.6:c.8160_8162dup (ATM) ENSP00000388058.2:p.Asp2721_Leu2722insAsp
ENST00000524755.5:c.227-560_227-558dup (C11orf65)
ENST00000524792.5:n.4375_4377dup (ATM)
ENST00000525056.1:n.357_359dup (ATM)
ENST00000525729.5:c.641-26781_641-26779dup (C11orf65) ENSP00000433395.1:n.641-26781_641-26779dup
ENST00000527531.5:c.*1197-560_*1197-558dup (C11orf65) ENSP00000431706.1:n.*1197-560_*1197-558dup
ENST00000533979.5:n.372_374dup (ATM)
ENST00000615746.4:c.*1197-560_*1197-558dup (C11orf65) ENSP00000483537.1:n.*1197-560_*1197-558dup
NM_000051.3:c.8160_8162dup , LRG_135t1:c.8160_8162dup (ATM) NP_000042.3:p.Asp2721_Leu2722insAsp
XM_005271414.3:c.788-560_788-558dup (C11orf65) XP_005271471.1:n.788-560_788-558dup
XM_005271415.3:c.732-560_732-558dup (C11orf65) XP_005271472.1:n.732-560_732-558dup
XM_005271561.3:c.8160_8162dup (ATM) XP_005271618.2:p.Asp2721_Leu2722insAsp
XM_005271562.3:c.8160_8162dup (ATM) XP_005271619.2:p.Asp2721_Leu2722insAsp
XM_006718843.2:c.8160_8162dup (ATM) XP_006718906.1:p.Asp2721_Leu2722insAsp
XM_006718845.1:c.4116_4118dup (ATM) XP_006718908.1:p.Asp1373_Leu1374insAsp
XM_011542840.1:c.8160_8162dup (ATM) XP_011541142.1:p.Asp2721_Leu2722insAsp
XM_011542841.1:c.8160_8162dup (ATM) XP_011541143.1:p.Asp2721_Leu2722insAsp
XM_011542842.1:c.7995_7997dup (ATM) XP_011541144.1:p.Asp2666_Leu2667insAsp
XM_011542843.1:c.8160_8162dup (ATM) XP_011541145.1:p.Asp2721_Leu2722insAsp
XM_011542844.1:c.7116_7118dup (ATM) XP_011541146.1:p.Asp2373_Leu2374insAsp
XM_011542845.1:c.6852_6854dup (ATM) XP_011541147.1:p.Asp2285_Leu2286insAsp
XM_011542847.1:c.3231_3233dup (ATM) XP_011541149.1:p.Asp1078_Leu1079insAsp
NM_001330368.1:c.641-26781_641-26779dup (C11orf65) NP_001317297.1:n.641-26781_641-26779dup
NM_001351110.1:c.695-560_695-558dup (C11orf65) NP_001338039.1:n.695-560_695-558dup
NM_001351834.1:c.8160_8162dup (ATM) NP_001338763.1:p.Asp2721_Leu2722insAsp
NR_147053.2:n.2302-560_2302-558dup (C11orf65)
XM_005271414.4:c.788-560_788-558dup (C11orf65) XP_005271471.1:n.788-560_788-558dup
XM_005271415.4:c.732-560_732-558dup (C11orf65) XP_005271472.1:n.732-560_732-558dup
XM_005271562.5:c.8160_8162dup (ATM) XP_005271619.2:p.Asp2721_Leu2722insAsp
XM_006718843.4:c.8160_8162dup (ATM) XP_006718906.1:p.Asp2721_Leu2722insAsp
XM_006718845.2:c.4116_4118dup (ATM) XP_006718908.1:p.Asp1373_Leu1374insAsp
XM_011542840.3:c.8160_8162dup (ATM) XP_011541142.1:p.Asp2721_Leu2722insAsp
XM_011542842.3:c.7995_7997dup (ATM) XP_011541144.1:p.Asp2666_Leu2667insAsp
XM_011542843.2:c.8160_8162dup (ATM) XP_011541145.1:p.Asp2721_Leu2722insAsp
XM_011542844.3:c.7116_7118dup (ATM) XP_011541146.1:p.Asp2373_Leu2374insAsp
XM_011542845.2:c.6852_6854dup (ATM) XP_011541147.1:p.Asp2285_Leu2286insAsp
XM_017017789.2:c.8160_8162dup (ATM) XP_016873278.1:p.Asp2721_Leu2722insAsp
XM_017017790.2:c.8160_8162dup (ATM) XP_016873279.1:p.Asp2721_Leu2722insAsp
NM_001330368.2:c.641-26781_641-26779dup (C11orf65) NP_001317297.1:n.641-26781_641-26779dup
NM_001351110.2:c.695-560_695-558dup (C11orf65) NP_001338039.1:n.695-560_695-558dup
NM_001351834.2:c.8160_8162dup (ATM) NP_001338763.1:p.Asp2721_Leu2722insAsp
NM_000051.4:c.8160_8162dup (ATM) MANE Select NP_000042.3:p.Asp2721_Leu2722insAsp
NR_147053.3:n.2300-560_2300-558dup (C11orf65)