Canonical Allele Identifier: CA1998800908

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108315894_108315895delinsGT , CM000673.2:g.108315894_108315895delinsGT	GRCh38
NC_000011.9:g.108186621_108186622delinsGT , CM000673.1:g.108186621_108186622delinsGT	GRCh37
NC_000011.8:g.107691831_107691832delinsGT	NCBI36
NG_009830.1:g.98063_98064delinsGT , LRG_135:g.98063_98064delinsGT
NG_054724.1:g.158938_158939delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6078_6079delinsGT (ATM)	ENSP00000388058.2:p.Met2026=
ENST00000713593.1:c.*5549_*5550delinsGT (ATM)	ENSP00000518889.1:n.*5549_*5550delinsGT
ENST00000278616.9:c.6078_6079delinsGT (ATM)	ENSP00000278616.4:p.Met2026=
ENST00000525056.2:n.497_498delinsGT (ATM)
ENST00000682286.1:n.835_836delinsGT (ATM)
ENST00000682302.1:n.496_497delinsGT (ATM)
ENST00000683174.1:n.7562_7563delinsGT (ATM)
ENST00000683524.1:n.1302_1303delinsGT (ATM)
ENST00000684152.1:n.1792_1793delinsGT (ATM)
ENST00000527805.6:c.*1142_*1143delinsGT (ATM)	ENSP00000435747.2:n.*1142_*1143delinsGT
ENST00000675595.1:c.*1142_*1143delinsGT (ATM)	ENSP00000502563.1:n.*1142_*1143delinsGT
ENST00000675843.1:c.6078_6079delinsGT (ATM) MANE Select	ENSP00000501606.1:p.Met2026=
ENST00000278616.8:c.6078_6079delinsGT (ATM)	ENSP00000278616.4:p.Met2026=
ENST00000452508.6:c.6078_6079delinsGT (ATM)	ENSP00000388058.2:p.Met2026=
ENST00000524792.5:n.2293_2294delinsGT (ATM)
ENST00000525729.5:c.641-6824_641-6823delinsAC (C11orf65)	ENSP00000433395.1:n.641-6824_641-6823delinsAC
ENST00000532765.1:n.395_396delinsGT (ATM)
ENST00000533690.5:n.1482_1483delinsGT (ATM)
NM_000051.3:c.6078_6079delinsGT , LRG_135t1:c.6078_6079delinsGT (ATM)	NP_000042.3:p.Met2026=
XM_005271561.3:c.6078_6079delinsGT (ATM)	XP_005271618.2:p.Met2026=
XM_005271562.3:c.6078_6079delinsGT (ATM)	XP_005271619.2:p.Met2026=
XM_006718843.2:c.6078_6079delinsGT (ATM)	XP_006718906.1:p.Met2026=
XM_006718845.1:c.2034_2035delinsGT (ATM)	XP_006718908.1:p.Met678=
XM_011542840.1:c.6078_6079delinsGT (ATM)	XP_011541142.1:p.Met2026=
XM_011542841.1:c.6078_6079delinsGT (ATM)	XP_011541143.1:p.Met2026=
XM_011542842.1:c.5913_5914delinsGT (ATM)	XP_011541144.1:p.Met1971=
XM_011542843.1:c.6078_6079delinsGT (ATM)	XP_011541145.1:p.Met2026=
XM_011542844.1:c.5034_5035delinsGT (ATM)	XP_011541146.1:p.Met1678=
XM_011542845.1:c.4770_4771delinsGT (ATM)	XP_011541147.1:p.Met1590=
XM_011542847.1:c.1149_1150delinsGT (ATM)	XP_011541149.1:p.Met383=
NM_001330368.1:c.641-6824_641-6823delinsAC (C11orf65)	NP_001317297.1:n.641-6824_641-6823delinsAC
NM_001351110.1:c.*39-6824_*39-6823delinsAC (C11orf65)	NP_001338039.1:n.*39-6824_*39-6823delinsAC
NM_001351834.1:c.6078_6079delinsGT (ATM)	NP_001338763.1:p.Met2026=
XM_005271562.5:c.6078_6079delinsGT (ATM)	XP_005271619.2:p.Met2026=
XM_006718843.4:c.6078_6079delinsGT (ATM)	XP_006718906.1:p.Met2026=
XM_006718845.2:c.2034_2035delinsGT (ATM)	XP_006718908.1:p.Met678=
XM_011542840.3:c.6078_6079delinsGT (ATM)	XP_011541142.1:p.Met2026=
XM_011542842.3:c.5913_5914delinsGT (ATM)	XP_011541144.1:p.Met1971=
XM_011542843.2:c.6078_6079delinsGT (ATM)	XP_011541145.1:p.Met2026=
XM_011542844.3:c.5034_5035delinsGT (ATM)	XP_011541146.1:p.Met1678=
XM_011542845.2:c.4770_4771delinsGT (ATM)	XP_011541147.1:p.Met1590=
XM_017017789.2:c.6078_6079delinsGT (ATM)	XP_016873278.1:p.Met2026=
XM_017017790.2:c.6078_6079delinsGT (ATM)	XP_016873279.1:p.Met2026=
XM_017017791.1:c.6078_6079delinsGT (ATM)	XP_016873280.1:p.Met2026=
NM_001330368.2:c.641-6824_641-6823delinsAC (C11orf65)	NP_001317297.1:n.641-6824_641-6823delinsAC
NM_001351110.2:c.*39-6824_*39-6823delinsAC (C11orf65)	NP_001338039.1:n.*39-6824_*39-6823delinsAC
NM_001351834.2:c.6078_6079delinsGT (ATM)	NP_001338763.1:p.Met2026=
NM_000051.4:c.6078_6079delinsGT (ATM) MANE Select	NP_000042.3:p.Met2026=