Canonical Allele Identifier: CA1998811061

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108332764_108332768delinsTCGAA , CM000673.2:g.108332764_108332768delinsTCGAA	GRCh38
NC_000011.9:g.108203491_108203495delinsTCGAA , CM000673.1:g.108203491_108203495delinsTCGAA	GRCh37
NC_000011.8:g.107708701_107708705delinsTCGAA	NCBI36
NG_009830.1:g.114933_114937delinsTCGAA , LRG_135:g.114933_114937delinsTCGAA
NG_054724.1:g.142065_142069delinsTTCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7791_7795delinsTCGAA (ATM)	ENSP00000388058.2:p.Asp2597=
ENST00000713593.1:c.*7262_*7266delinsTCGAA (ATM)	ENSP00000518889.1:n.*7262_*7266delinsTCGAA
ENST00000278616.9:c.7791_7795delinsTCGAA (ATM)	ENSP00000278616.4:p.Asp2597=
ENST00000525056.2:n.2210_2214delinsTCGAA (ATM)
ENST00000525537.3:n.1472_1476delinsTCGAA (ATM)
ENST00000638786.2:n.625+727_625+731delinsTCGAA (ATM)
ENST00000682286.1:n.2548_2552delinsTCGAA (ATM)
ENST00000682302.1:n.2209_2213delinsTCGAA (ATM)
ENST00000683174.1:n.9275_9279delinsTCGAA (ATM)
ENST00000683524.1:n.3015_3019delinsTCGAA (ATM)
ENST00000684152.1:n.3344-1122_3344-1118delinsTCGAA (ATM)
ENST00000684180.1:n.265_269delinsTCGAA (ATM)
ENST00000684447.1:n.3299_3303delinsTCGAA (ATM)
ENST00000527805.6:c.*2855_*2859delinsTCGAA (ATM)	ENSP00000435747.2:n.*2855_*2859delinsTCGAA
ENST00000675595.1:c.*2926_*2930delinsTCGAA (ATM)	ENSP00000502563.1:n.*2926_*2930delinsTCGAA
ENST00000675843.1:c.7791_7795delinsTCGAA (ATM) MANE Select	ENSP00000501606.1:p.Asp2597=
ENST00000278616.8:c.7791_7795delinsTCGAA (ATM)	ENSP00000278616.4:p.Asp2597=
ENST00000452508.6:c.7791_7795delinsTCGAA (ATM)	ENSP00000388058.2:p.Asp2597=
ENST00000524755.5:c.300-1201_300-1197delinsTTCGA (C11orf65)
ENST00000524792.5:n.4006_4010delinsTCGAA (ATM)
ENST00000525729.5:c.641-23697_641-23693delinsTTCGA (C11orf65)	ENSP00000433395.1:n.641-23697_641-23693delinsTTCGA
ENST00000527531.5:c.*1270-1201_*1270-1197delinsTTCGA (C11orf65)	ENSP00000431706.1:n.*1270-1201_*1270-1197delinsTTCGA
ENST00000533690.5:n.3195_3199delinsTCGAA (ATM)
ENST00000533979.5:n.3_7delinsTCGAA (ATM)
ENST00000615746.4:c.*1270-1201_*1270-1197delinsTTCGA (C11orf65)	ENSP00000483537.1:n.*1270-1201_*1270-1197delinsTTCGA
NM_000051.3:c.7791_7795delinsTCGAA , LRG_135t1:c.7791_7795delinsTCGAA (ATM)	NP_000042.3:p.Asp2597=
XM_005271414.3:c.*39-1201_*39-1197delinsTTCGA (C11orf65)	XP_005271471.1:n.*39-1201_*39-1197delinsTTCGA
XM_005271415.3:c.805-1201_805-1197delinsTTCGA (C11orf65)	XP_005271472.1:n.805-1201_805-1197delinsTTCGA
XM_005271561.3:c.7791_7795delinsTCGAA (ATM)	XP_005271618.2:p.Asp2597=
XM_005271562.3:c.7791_7795delinsTCGAA (ATM)	XP_005271619.2:p.Asp2597=
XM_006718843.2:c.7791_7795delinsTCGAA (ATM)	XP_006718906.1:p.Asp2597=
XM_006718845.1:c.3747_3751delinsTCGAA (ATM)	XP_006718908.1:p.Asp1249=
XM_011542840.1:c.7791_7795delinsTCGAA (ATM)	XP_011541142.1:p.Asp2597=
XM_011542841.1:c.7791_7795delinsTCGAA (ATM)	XP_011541143.1:p.Asp2597=
XM_011542842.1:c.7626_7630delinsTCGAA (ATM)	XP_011541144.1:p.Asp2542=
XM_011542843.1:c.7791_7795delinsTCGAA (ATM)	XP_011541145.1:p.Asp2597=
XM_011542844.1:c.6747_6751delinsTCGAA (ATM)	XP_011541146.1:p.Asp2249=
XM_011542845.1:c.6483_6487delinsTCGAA (ATM)	XP_011541147.1:p.Asp2161=
XM_011542847.1:c.2862_2866delinsTCGAA (ATM)	XP_011541149.1:p.Asp954=
NM_001330368.1:c.641-23697_641-23693delinsTTCGA (C11orf65)	NP_001317297.1:n.641-23697_641-23693delinsTTCGA
NM_001351110.1:c.*38+2452_*38+2456delinsTTCGA (C11orf65)	NP_001338039.1:n.*38+2452_*38+2456delinsTTCGA
NM_001351834.1:c.7791_7795delinsTCGAA (ATM)	NP_001338763.1:p.Asp2597=
NR_147053.2:n.2375-1201_2375-1197delinsTTCGA (C11orf65)
XM_005271414.4:c.*39-1201_*39-1197delinsTTCGA (C11orf65)	XP_005271471.1:n.*39-1201_*39-1197delinsTTCGA
XM_005271415.4:c.805-1201_805-1197delinsTTCGA (C11orf65)	XP_005271472.1:n.805-1201_805-1197delinsTTCGA
XM_005271562.5:c.7791_7795delinsTCGAA (ATM)	XP_005271619.2:p.Asp2597=
XM_006718843.4:c.7791_7795delinsTCGAA (ATM)	XP_006718906.1:p.Asp2597=
XM_006718845.2:c.3747_3751delinsTCGAA (ATM)	XP_006718908.1:p.Asp1249=
XM_011542840.3:c.7791_7795delinsTCGAA (ATM)	XP_011541142.1:p.Asp2597=
XM_011542842.3:c.7626_7630delinsTCGAA (ATM)	XP_011541144.1:p.Asp2542=
XM_011542843.2:c.7791_7795delinsTCGAA (ATM)	XP_011541145.1:p.Asp2597=
XM_011542844.3:c.6747_6751delinsTCGAA (ATM)	XP_011541146.1:p.Asp2249=
XM_011542845.2:c.6483_6487delinsTCGAA (ATM)	XP_011541147.1:p.Asp2161=
XM_017017789.2:c.7791_7795delinsTCGAA (ATM)	XP_016873278.1:p.Asp2597=
XM_017017790.2:c.7791_7795delinsTCGAA (ATM)	XP_016873279.1:p.Asp2597=
NM_001330368.2:c.641-23697_641-23693delinsTTCGA (C11orf65)	NP_001317297.1:n.641-23697_641-23693delinsTTCGA
NM_001351110.2:c.*38+2452_*38+2456delinsTTCGA (C11orf65)	NP_001338039.1:n.*38+2452_*38+2456delinsTTCGA
NM_001351834.2:c.7791_7795delinsTCGAA (ATM)	NP_001338763.1:p.Asp2597=
NM_000051.4:c.7791_7795delinsTCGAA (ATM) MANE Select	NP_000042.3:p.Asp2597=
NR_147053.3:n.2373-1201_2373-1197delinsTTCGA (C11orf65)