Canonical Allele Identifier: CA382530890

Gene: ATM C11orf65

Linked Data

• dbSNP Id: rs534644067
• MyVariant Identifiers: chr11:g.108236068T>C (hg19) ; chr11:g.108365341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108365341T>C , CM000673.2:g.108365341T>C	GRCh38
NC_000011.9:g.108236068T>C , CM000673.1:g.108236068T>C	GRCh37
NC_000011.8:g.107741278T>C	NCBI36
NG_009830.1:g.147510T>C , LRG_135:g.147510T>C
NG_054724.1:g.109492A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.9004T>C (ATM)	ENSP00000388058.2:p.Phe3002Leu
ENST00000713593.1:c.*8475T>C (ATM)	ENSP00000518889.1:n.*8475T>C
ENST00000278616.9:c.9004T>C (ATM)	ENSP00000278616.4:p.Phe3002Leu
ENST00000638786.2:n.1702T>C (ATM)
ENST00000682286.1:n.3761T>C (ATM)
ENST00000682302.1:n.3422T>C (ATM)
ENST00000682569.1:n.2351T>C (ATM)
ENST00000683174.1:n.10488T>C (ATM)
ENST00000683524.1:n.4228T>C (ATM)
ENST00000684152.1:n.4420T>C (ATM)
ENST00000684180.1:n.1478T>C (ATM)
ENST00000684447.1:n.5497T>C (ATM)
ENST00000527805.6:c.*4068T>C (ATM)	ENSP00000435747.2:n.*4068T>C
ENST00000675595.1:c.*4139T>C (ATM)	ENSP00000502563.1:n.*4139T>C
ENST00000675843.1:c.9004T>C (ATM) MANE Select	ENSP00000501606.1:p.Phe3002Leu
ENST00000278616.8:c.9004T>C (ATM)	ENSP00000278616.4:p.Phe3002Leu
ENST00000452508.6:c.9004T>C (ATM)	ENSP00000388058.2:p.Phe3002Leu
ENST00000524755.5:c.226+27867A>G (C11orf65)
ENST00000524792.5:n.5219T>C (ATM)
ENST00000525178.5:n.492T>C (ATM)
ENST00000525729.5:c.640+20579A>G (C11orf65)	ENSP00000433395.1:n.640+20579A>G
ENST00000526725.1:n.272-24977A>G (C11orf65)
ENST00000527181.1:n.343T>C (ATM)
ENST00000527531.5:c.*2-9232A>G (C11orf65)	ENSP00000431706.1:n.*2-9232A>G
ENST00000615746.4:c.*2-9232A>G (C11orf65)	ENSP00000483537.1:n.*2-9232A>G
NM_000051.3:c.9004T>C , LRG_135t1:c.9004T>C (ATM)	NP_000042.3:p.Phe3002Leu
XM_005271414.3:c.787+20579A>G (C11orf65)	XP_005271471.1:n.787+20579A>G
XM_005271415.3:c.731+27867A>G (C11orf65)	XP_005271472.1:n.731+27867A>G
XM_005271561.3:c.9004T>C (ATM)	XP_005271618.2:p.Phe3002Leu
XM_005271562.3:c.9004T>C (ATM)	XP_005271619.2:p.Phe3002Leu
XM_006718843.2:c.9004T>C (ATM)	XP_006718906.1:p.Phe3002Leu
XM_006718845.1:c.4960T>C (ATM)	XP_006718908.1:p.Phe1654Leu
XM_011542640.1:c.787+20579A>G (C11orf65)	XP_011540942.1:n.787+20579A>G
XM_011542642.1:c.732-16268A>G (C11orf65)	XP_011540944.1:n.732-16268A>G
XM_011542643.1:c.732-24977A>G (C11orf65)	XP_011540945.1:n.732-24977A>G
XM_011542840.1:c.9004T>C (ATM)	XP_011541142.1:p.Phe3002Leu
XM_011542841.1:c.9004T>C (ATM)	XP_011541143.1:p.Phe3002Leu
XM_011542842.1:c.8839T>C (ATM)	XP_011541144.1:p.Phe2947Leu
XM_011542844.1:c.7960T>C (ATM)	XP_011541146.1:p.Phe2654Leu
XM_011542845.1:c.7696T>C (ATM)	XP_011541147.1:p.Phe2566Leu
XM_011542847.1:c.4075T>C (ATM)	XP_011541149.1:p.Phe1359Leu
NM_001330368.1:c.640+20579A>G (C11orf65)	NP_001317297.1:n.640+20579A>G
NM_001351110.1:c.694+20579A>G (C11orf65)	NP_001338039.1:n.694+20579A>G
NM_001351834.1:c.9004T>C (ATM)	NP_001338763.1:p.Phe3002Leu
NR_147053.2:n.1107-9232A>G (C11orf65)
XM_005271414.4:c.787+20579A>G (C11orf65)	XP_005271471.1:n.787+20579A>G
XM_005271415.4:c.731+27867A>G (C11orf65)	XP_005271472.1:n.731+27867A>G
XM_005271562.5:c.9004T>C (ATM)	XP_005271619.2:p.Phe3002Leu
XM_006718843.4:c.9004T>C (ATM)	XP_006718906.1:p.Phe3002Leu
XM_006718845.2:c.4960T>C (ATM)	XP_006718908.1:p.Phe1654Leu
XM_011542640.2:c.787+20579A>G (C11orf65)	XP_011540942.1:n.787+20579A>G
XM_011542643.2:c.732-24977A>G (C11orf65)	XP_011540945.1:n.732-24977A>G
XM_011542840.3:c.9004T>C (ATM)	XP_011541142.1:p.Phe3002Leu
XM_011542842.3:c.8839T>C (ATM)	XP_011541144.1:p.Phe2947Leu
XM_011542844.3:c.7960T>C (ATM)	XP_011541146.1:p.Phe2654Leu
XM_011542845.2:c.7696T>C (ATM)	XP_011541147.1:p.Phe2566Leu
XM_017017247.1:c.903+17719A>G (C11orf65)	XP_016872736.1:n.903+17719A>G
XM_017017789.2:c.9004T>C (ATM)	XP_016873278.1:p.Phe3002Leu
XM_017017790.2:c.9004T>C (ATM)	XP_016873279.1:p.Phe3002Leu
NM_001330368.2:c.640+20579A>G (C11orf65)	NP_001317297.1:n.640+20579A>G
NM_001351110.2:c.694+20579A>G (C11orf65)	NP_001338039.1:n.694+20579A>G
NM_001351834.2:c.9004T>C (ATM)	NP_001338763.1:p.Phe3002Leu
NM_000051.4:c.9004T>C (ATM) MANE Select	NP_000042.3:p.Phe3002Leu
NR_147053.3:n.1105-9232A>G (C11orf65)