Canonical Allele Identifier: CA382523722

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 822671
• ClinVar RCV Id: RCV001018207 ; RCV001059139
• dbSNP Id: rs1591306636
• MyVariant Identifiers: chr11:g.108224526C>T (hg19) ; chr11:g.108353799C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108353799C>T , CM000673.2:g.108353799C>T	GRCh38
NC_000011.9:g.108224526C>T , CM000673.1:g.108224526C>T	GRCh37
NC_000011.8:g.107729736C>T	NCBI36
NG_009830.1:g.135968C>T , LRG_135:g.135968C>T
NG_054724.1:g.121034G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8705C>T (ATM)	ENSP00000388058.2:p.Thr2902Ile
ENST00000713593.1:c.*8176C>T (ATM)	ENSP00000518889.1:n.*8176C>T
ENST00000278616.9:c.8705C>T (ATM)	ENSP00000278616.4:p.Thr2902Ile
ENST00000638786.2:n.1403C>T (ATM)
ENST00000682286.1:n.3462C>T (ATM)
ENST00000682302.1:n.3123C>T (ATM)
ENST00000683174.1:n.10189C>T (ATM)
ENST00000683524.1:n.3929C>T (ATM)
ENST00000684152.1:n.4121C>T (ATM)
ENST00000684180.1:n.1179C>T (ATM)
ENST00000684447.1:n.5198C>T (ATM)
ENST00000527805.6:c.*3769C>T (ATM)	ENSP00000435747.2:n.*3769C>T
ENST00000675595.1:c.*3840C>T (ATM)	ENSP00000502563.1:n.*3840C>T
ENST00000675843.1:c.8705C>T (ATM) MANE Select	ENSP00000501606.1:p.Thr2902Ile
ENST00000278616.8:c.8705C>T (ATM)	ENSP00000278616.4:p.Thr2902Ile
ENST00000452508.6:c.8705C>T (ATM)	ENSP00000388058.2:p.Thr2902Ile
ENST00000524755.5:c.227-18507G>A (C11orf65)
ENST00000524792.5:n.4920C>T (ATM)
ENST00000525178.5:n.193C>T (ATM)
ENST00000525729.5:c.640+32121G>A (C11orf65)	ENSP00000433395.1:n.640+32121G>A
ENST00000526725.1:n.272-13435G>A (C11orf65)
ENST00000527181.1:n.44C>T (ATM)
ENST00000527531.5:c.*1196+1116G>A (C11orf65)	ENSP00000431706.1:n.*1196+1116G>A
ENST00000615746.4:c.*1196+1116G>A (C11orf65)	ENSP00000483537.1:n.*1196+1116G>A
NM_000051.3:c.8705C>T , LRG_135t1:c.8705C>T (ATM)	NP_000042.3:p.Thr2902Ile
XM_005271414.3:c.788-18507G>A (C11orf65)	XP_005271471.1:n.788-18507G>A
XM_005271415.3:c.732-18507G>A (C11orf65)	XP_005271472.1:n.732-18507G>A
XM_005271561.3:c.8705C>T (ATM)	XP_005271618.2:p.Thr2902Ile
XM_005271562.3:c.8705C>T (ATM)	XP_005271619.2:p.Thr2902Ile
XM_006718843.2:c.8705C>T (ATM)	XP_006718906.1:p.Thr2902Ile
XM_006718845.1:c.4661C>T (ATM)	XP_006718908.1:p.Thr1554Ile
XM_011542640.1:c.788-13435G>A (C11orf65)	XP_011540942.1:n.788-13435G>A
XM_011542642.1:c.732-4726G>A (C11orf65)	XP_011540944.1:n.732-4726G>A
XM_011542643.1:c.732-13435G>A (C11orf65)	XP_011540945.1:n.732-13435G>A
XM_011542840.1:c.8705C>T (ATM)	XP_011541142.1:p.Thr2902Ile
XM_011542841.1:c.8705C>T (ATM)	XP_011541143.1:p.Thr2902Ile
XM_011542842.1:c.8540C>T (ATM)	XP_011541144.1:p.Thr2847Ile
XM_011542844.1:c.7661C>T (ATM)	XP_011541146.1:p.Thr2554Ile
XM_011542845.1:c.7397C>T (ATM)	XP_011541147.1:p.Thr2466Ile
XM_011542847.1:c.3776C>T (ATM)	XP_011541149.1:p.Thr1259Ile
NM_001330368.1:c.640+32121G>A (C11orf65)	NP_001317297.1:n.640+32121G>A
NM_001351110.1:c.695-18507G>A (C11orf65)	NP_001338039.1:n.695-18507G>A
NM_001351834.1:c.8705C>T (ATM)	NP_001338763.1:p.Thr2902Ile
NR_147053.2:n.2301+1116G>A (C11orf65)
XM_005271414.4:c.788-18507G>A (C11orf65)	XP_005271471.1:n.788-18507G>A
XM_005271415.4:c.732-18507G>A (C11orf65)	XP_005271472.1:n.732-18507G>A
XM_005271562.5:c.8705C>T (ATM)	XP_005271619.2:p.Thr2902Ile
XM_006718843.4:c.8705C>T (ATM)	XP_006718906.1:p.Thr2902Ile
XM_006718845.2:c.4661C>T (ATM)	XP_006718908.1:p.Thr1554Ile
XM_011542640.2:c.788-13435G>A (C11orf65)	XP_011540942.1:n.788-13435G>A
XM_011542643.2:c.732-13435G>A (C11orf65)	XP_011540945.1:n.732-13435G>A
XM_011542840.3:c.8705C>T (ATM)	XP_011541142.1:p.Thr2902Ile
XM_011542842.3:c.8540C>T (ATM)	XP_011541144.1:p.Thr2847Ile
XM_011542844.3:c.7661C>T (ATM)	XP_011541146.1:p.Thr2554Ile
XM_011542845.2:c.7397C>T (ATM)	XP_011541147.1:p.Thr2466Ile
XM_017017247.1:c.904-13435G>A (C11orf65)	XP_016872736.1:n.904-13435G>A
XM_017017789.2:c.8705C>T (ATM)	XP_016873278.1:p.Thr2902Ile
XM_017017790.2:c.8705C>T (ATM)	XP_016873279.1:p.Thr2902Ile
NM_001330368.2:c.640+32121G>A (C11orf65)	NP_001317297.1:n.640+32121G>A
NM_001351110.2:c.695-18507G>A (C11orf65)	NP_001338039.1:n.695-18507G>A
NM_001351834.2:c.8705C>T (ATM)	NP_001338763.1:p.Thr2902Ile
NM_000051.4:c.8705C>T (ATM) MANE Select	NP_000042.3:p.Thr2902Ile
NR_147053.3:n.2299+1116G>A (C11orf65)