Canonical Allele Identifier: CA382561879

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108334989T>G , CM000673.2:g.108334989T>G	GRCh38
NC_000011.9:g.108205716T>G , CM000673.1:g.108205716T>G	GRCh37
NC_000011.8:g.107710926T>G	NCBI36
NG_009830.1:g.117158T>G , LRG_135:g.117158T>G
NG_054724.1:g.139844A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000051.4:c.8031T>G (ATM) MANE Select	NP_000042.3:p.Tyr2677Ter
ENST00000675843.1:c.8031T>G (ATM) MANE Select	ENSP00000501606.1:p.Tyr2677Ter
NM_000051.3:c.8031T>G , LRG_135t1:c.8031T>G (ATM)	NP_000042.3:p.Tyr2677Ter
NM_001330368.1:c.641-25918A>C (C11orf65)	NP_001317297.1:n.641-25918A>C
NM_001330368.2:c.641-25918A>C (C11orf65)	NP_001317297.1:n.641-25918A>C
NM_001351110.1:c.*38+231A>C (C11orf65)	NP_001338039.1:n.*38+231A>C
NM_001351110.2:c.*38+231A>C (C11orf65)	NP_001338039.1:n.*38+231A>C
NM_001351834.1:c.8031T>G (ATM)	NP_001338763.1:p.Tyr2677Ter
NM_001351834.2:c.8031T>G (ATM)	NP_001338763.1:p.Tyr2677Ter
NR_147053.2:n.2374+231A>C (C11orf65)
NR_147053.3:n.2372+231A>C (C11orf65)
ENST00000278616.8:c.8031T>G (ATM)	ENSP00000278616.4:p.Tyr2677Ter
ENST00000278616.9:c.8031T>G (ATM)	ENSP00000278616.4:p.Tyr2677Ter
ENST00000452508.6:c.8031T>G (ATM)	ENSP00000388058.2:p.Tyr2677Ter
ENST00000452508.7:c.8031T>G (ATM)	ENSP00000388058.2:p.Tyr2677Ter
ENST00000524755.5:c.299+231A>C (C11orf65)
ENST00000524792.5:n.4246T>G (ATM)
ENST00000525056.1:n.228T>G (ATM)
ENST00000525056.2:n.2450T>G (ATM)
ENST00000525729.5:c.641-25918A>C (C11orf65)	ENSP00000433395.1:n.641-25918A>C
ENST00000527531.5:c.*1269+231A>C (C11orf65)	ENSP00000431706.1:n.*1269+231A>C
ENST00000527805.6:c.*3095T>G (ATM)	ENSP00000435747.2:n.*3095T>G
ENST00000533979.5:n.243T>G (ATM)
ENST00000615746.4:c.*1269+231A>C (C11orf65)	ENSP00000483537.1:n.*1269+231A>C
ENST00000638786.2:n.729T>G (ATM)
ENST00000675595.1:c.*3166T>G (ATM)	ENSP00000502563.1:n.*3166T>G
ENST00000682286.1:n.2788T>G (ATM)
ENST00000682302.1:n.2449T>G (ATM)
ENST00000683174.1:n.9515T>G (ATM)
ENST00000683524.1:n.3255T>G (ATM)
ENST00000684152.1:n.3447T>G (ATM)
ENST00000684180.1:n.505T>G (ATM)
ENST00000684447.1:n.4524T>G (ATM)
ENST00000713593.1:c.*7502T>G (ATM)	ENSP00000518889.1:n.*7502T>G
XM_005271414.3:c.*38+231A>C (C11orf65)	XP_005271471.1:n.*38+231A>C
XM_005271414.4:c.*38+231A>C (C11orf65)	XP_005271471.1:n.*38+231A>C
XM_005271415.3:c.804+231A>C (C11orf65)	XP_005271472.1:n.804+231A>C
XM_005271415.4:c.804+231A>C (C11orf65)	XP_005271472.1:n.804+231A>C
XM_005271561.3:c.8031T>G (ATM)	XP_005271618.2:p.Tyr2677Ter
XM_005271562.3:c.8031T>G (ATM)	XP_005271619.2:p.Tyr2677Ter
XM_005271562.5:c.8031T>G (ATM)	XP_005271619.2:p.Tyr2677Ter
XM_006718843.2:c.8031T>G (ATM)	XP_006718906.1:p.Tyr2677Ter
XM_006718843.4:c.8031T>G (ATM)	XP_006718906.1:p.Tyr2677Ter
XM_006718845.1:c.3987T>G (ATM)	XP_006718908.1:p.Tyr1329Ter
XM_006718845.2:c.3987T>G (ATM)	XP_006718908.1:p.Tyr1329Ter
XM_011542840.1:c.8031T>G (ATM)	XP_011541142.1:p.Tyr2677Ter
XM_011542840.3:c.8031T>G (ATM)	XP_011541142.1:p.Tyr2677Ter
XM_011542841.1:c.8031T>G (ATM)	XP_011541143.1:p.Tyr2677Ter
XM_011542842.1:c.7866T>G (ATM)	XP_011541144.1:p.Tyr2622Ter
XM_011542842.3:c.7866T>G (ATM)	XP_011541144.1:p.Tyr2622Ter
XM_011542843.1:c.8031T>G (ATM)	XP_011541145.1:p.Tyr2677Ter
XM_011542843.2:c.8031T>G (ATM)	XP_011541145.1:p.Tyr2677Ter
XM_011542844.1:c.6987T>G (ATM)	XP_011541146.1:p.Tyr2329Ter
XM_011542844.3:c.6987T>G (ATM)	XP_011541146.1:p.Tyr2329Ter
XM_011542845.1:c.6723T>G (ATM)	XP_011541147.1:p.Tyr2241Ter
XM_011542845.2:c.6723T>G (ATM)	XP_011541147.1:p.Tyr2241Ter
XM_011542847.1:c.3102T>G (ATM)	XP_011541149.1:p.Tyr1034Ter
XM_017017789.2:c.8031T>G (ATM)	XP_016873278.1:p.Tyr2677Ter
XM_017017790.2:c.8031T>G (ATM)	XP_016873279.1:p.Tyr2677Ter