Canonical Allele Identifier: CA476672630

Gene: ATM C11orf65

Linked Data

• dbSNP Id: rs2136945860
• MyVariant Identifiers: chr11:g.108214008T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108343281T>A , CM000673.2:g.108343281T>A	GRCh38
NC_000011.9:g.108214008T>A , CM000673.1:g.108214008T>A	GRCh37
NC_000011.8:g.107719218T>A	NCBI36
NG_009830.1:g.125450T>A , LRG_135:g.125450T>A
NG_054724.1:g.131552A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.8328T>A (ATM)	ENSP00000388058.2:p.Ile2776=
ENST00000713593.1:c.*7799T>A (ATM)	ENSP00000518889.1:n.*7799T>A
ENST00000278616.9:c.8328T>A (ATM)	ENSP00000278616.4:p.Ile2776=
ENST00000638786.2:n.1026T>A (ATM)
ENST00000682286.1:n.3085T>A (ATM)
ENST00000682302.1:n.2746T>A (ATM)
ENST00000683174.1:n.9812T>A (ATM)
ENST00000683524.1:n.3552T>A (ATM)
ENST00000684152.1:n.3744T>A (ATM)
ENST00000684180.1:n.802T>A (ATM)
ENST00000684447.1:n.4821T>A (ATM)
ENST00000527805.6:c.*3392T>A (ATM)	ENSP00000435747.2:n.*3392T>A
ENST00000675595.1:c.*3463T>A (ATM)	ENSP00000502563.1:n.*3463T>A
ENST00000675843.1:c.8328T>A (ATM) MANE Select	ENSP00000501606.1:p.Ile2776=
ENST00000278616.8:c.8328T>A (ATM)	ENSP00000278616.4:p.Ile2776=
ENST00000452508.6:c.8328T>A (ATM)	ENSP00000388058.2:p.Ile2776=
ENST00000524755.5:c.227-7989A>T (C11orf65)
ENST00000524792.5:n.4543T>A (ATM)
ENST00000525729.5:c.641-34210A>T (C11orf65)	ENSP00000433395.1:n.641-34210A>T
ENST00000526725.1:n.272-2917A>T (C11orf65)
ENST00000527531.5:c.*1197-7989A>T (C11orf65)	ENSP00000431706.1:n.*1197-7989A>T
ENST00000615746.4:c.*1197-7989A>T (C11orf65)	ENSP00000483537.1:n.*1197-7989A>T
NM_000051.3:c.8328T>A , LRG_135t1:c.8328T>A (ATM)	NP_000042.3:p.Ile2776=
XM_005271414.3:c.788-7989A>T (C11orf65)	XP_005271471.1:n.788-7989A>T
XM_005271415.3:c.732-7989A>T (C11orf65)	XP_005271472.1:n.732-7989A>T
XM_005271561.3:c.8328T>A (ATM)	XP_005271618.2:p.Ile2776=
XM_005271562.3:c.8328T>A (ATM)	XP_005271619.2:p.Ile2776=
XM_006718843.2:c.8328T>A (ATM)	XP_006718906.1:p.Ile2776=
XM_006718845.1:c.4284T>A (ATM)	XP_006718908.1:p.Ile1428=
XM_011542640.1:c.788-2917A>T (C11orf65)	XP_011540942.1:n.788-2917A>T
XM_011542643.1:c.732-2917A>T (C11orf65)	XP_011540945.1:n.732-2917A>T
XM_011542840.1:c.8328T>A (ATM)	XP_011541142.1:p.Ile2776=
XM_011542841.1:c.8328T>A (ATM)	XP_011541143.1:p.Ile2776=
XM_011542842.1:c.8163T>A (ATM)	XP_011541144.1:p.Ile2721=
XM_011542843.1:c.8328T>A (ATM)	XP_011541145.1:p.Ile2776=
XM_011542844.1:c.7284T>A (ATM)	XP_011541146.1:p.Ile2428=
XM_011542845.1:c.7020T>A (ATM)	XP_011541147.1:p.Ile2340=
XM_011542847.1:c.3399T>A (ATM)	XP_011541149.1:p.Ile1133=
NM_001330368.1:c.641-34210A>T (C11orf65)	NP_001317297.1:n.641-34210A>T
NM_001351110.1:c.695-7989A>T (C11orf65)	NP_001338039.1:n.695-7989A>T
NM_001351834.1:c.8328T>A (ATM)	NP_001338763.1:p.Ile2776=
NR_147053.2:n.2302-7989A>T (C11orf65)
XM_005271414.4:c.788-7989A>T (C11orf65)	XP_005271471.1:n.788-7989A>T
XM_005271415.4:c.732-7989A>T (C11orf65)	XP_005271472.1:n.732-7989A>T
XM_005271562.5:c.8328T>A (ATM)	XP_005271619.2:p.Ile2776=
XM_006718843.4:c.8328T>A (ATM)	XP_006718906.1:p.Ile2776=
XM_006718845.2:c.4284T>A (ATM)	XP_006718908.1:p.Ile1428=
XM_011542640.2:c.788-2917A>T (C11orf65)	XP_011540942.1:n.788-2917A>T
XM_011542643.2:c.732-2917A>T (C11orf65)	XP_011540945.1:n.732-2917A>T
XM_011542840.3:c.8328T>A (ATM)	XP_011541142.1:p.Ile2776=
XM_011542842.3:c.8163T>A (ATM)	XP_011541144.1:p.Ile2721=
XM_011542843.2:c.8328T>A (ATM)	XP_011541145.1:p.Ile2776=
XM_011542844.3:c.7284T>A (ATM)	XP_011541146.1:p.Ile2428=
XM_011542845.2:c.7020T>A (ATM)	XP_011541147.1:p.Ile2340=
XM_017017247.1:c.904-2917A>T (C11orf65)	XP_016872736.1:n.904-2917A>T
XM_017017789.2:c.8328T>A (ATM)	XP_016873278.1:p.Ile2776=
XM_017017790.2:c.8328T>A (ATM)	XP_016873279.1:p.Ile2776=
NM_001330368.2:c.641-34210A>T (C11orf65)	NP_001317297.1:n.641-34210A>T
NM_001351110.2:c.695-7989A>T (C11orf65)	NP_001338039.1:n.695-7989A>T
NM_001351834.2:c.8328T>A (ATM)	NP_001338763.1:p.Ile2776=
NM_000051.4:c.8328T>A (ATM) MANE Select	NP_000042.3:p.Ile2776=
NR_147053.3:n.2300-7989A>T (C11orf65)