Canonical Allele Identifier: CA166363

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 141766
• ClinVar RCV Id: RCV000130403 ; RCV000411562 ; RCV004019739
• dbSNP Id: rs587781994
• MyVariant Identifiers: chr11:g.108204636C>T (hg19) ; chr11:g.108333909C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108333909C>T , CM000673.2:g.108333909C>T	GRCh38
NC_000011.9:g.108204636C>T , CM000673.1:g.108204636C>T	GRCh37
NC_000011.8:g.107709846C>T	NCBI36
NG_009830.1:g.116078C>T , LRG_135:g.116078C>T
NG_054724.1:g.140924G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7951C>T (ATM)	ENSP00000388058.2:p.Gln2651Ter
ENST00000713593.1:c.*7422C>T (ATM)	ENSP00000518889.1:n.*7422C>T
ENST00000278616.9:c.7951C>T (ATM)	ENSP00000278616.4:p.Gln2651Ter
ENST00000525056.2:n.2370C>T (ATM)
ENST00000638786.2:n.649C>T (ATM)
ENST00000682286.1:n.2708C>T (ATM)
ENST00000682302.1:n.2369C>T (ATM)
ENST00000683174.1:n.9435C>T (ATM)
ENST00000683524.1:n.3175C>T (ATM)
ENST00000684152.1:n.3367C>T (ATM)
ENST00000684180.1:n.425C>T (ATM)
ENST00000684447.1:n.4444C>T (ATM)
ENST00000527805.6:c.*3015C>T (ATM)	ENSP00000435747.2:n.*3015C>T
ENST00000675595.1:c.*3086C>T (ATM)	ENSP00000502563.1:n.*3086C>T
ENST00000675843.1:c.7951C>T (ATM) MANE Select	ENSP00000501606.1:p.Gln2651Ter
ENST00000278616.8:c.7951C>T (ATM)	ENSP00000278616.4:p.Gln2651Ter
ENST00000452508.6:c.7951C>T (ATM)	ENSP00000388058.2:p.Gln2651Ter
ENST00000524755.5:c.299+1311G>A (C11orf65)
ENST00000524792.5:n.4166C>T (ATM)
ENST00000525056.1:n.148C>T (ATM)
ENST00000525729.5:c.641-24838G>A (C11orf65)	ENSP00000433395.1:n.641-24838G>A
ENST00000527531.5:c.*1269+1311G>A (C11orf65)	ENSP00000431706.1:n.*1269+1311G>A
ENST00000533979.5:n.163C>T (ATM)
ENST00000615746.4:c.*1269+1311G>A (C11orf65)	ENSP00000483537.1:n.*1269+1311G>A
NM_000051.3:c.7951C>T , LRG_135t1:c.7951C>T (ATM)	NP_000042.3:p.Gln2651Ter
XM_005271414.3:c.*38+1311G>A (C11orf65)	XP_005271471.1:n.*38+1311G>A
XM_005271415.3:c.804+1311G>A (C11orf65)	XP_005271472.1:n.804+1311G>A
XM_005271561.3:c.7951C>T (ATM)	XP_005271618.2:p.Gln2651Ter
XM_005271562.3:c.7951C>T (ATM)	XP_005271619.2:p.Gln2651Ter
XM_006718843.2:c.7951C>T (ATM)	XP_006718906.1:p.Gln2651Ter
XM_006718845.1:c.3907C>T (ATM)	XP_006718908.1:p.Gln1303Ter
XM_011542840.1:c.7951C>T (ATM)	XP_011541142.1:p.Gln2651Ter
XM_011542841.1:c.7951C>T (ATM)	XP_011541143.1:p.Gln2651Ter
XM_011542842.1:c.7786C>T (ATM)	XP_011541144.1:p.Gln2596Ter
XM_011542843.1:c.7951C>T (ATM)	XP_011541145.1:p.Gln2651Ter
XM_011542844.1:c.6907C>T (ATM)	XP_011541146.1:p.Gln2303Ter
XM_011542845.1:c.6643C>T (ATM)	XP_011541147.1:p.Gln2215Ter
XM_011542847.1:c.3022C>T (ATM)	XP_011541149.1:p.Gln1008Ter
NM_001330368.1:c.641-24838G>A (C11orf65)	NP_001317297.1:n.641-24838G>A
NM_001351110.1:c.*38+1311G>A (C11orf65)	NP_001338039.1:n.*38+1311G>A
NM_001351834.1:c.7951C>T (ATM)	NP_001338763.1:p.Gln2651Ter
NR_147053.2:n.2374+1311G>A (C11orf65)
XM_005271414.4:c.*38+1311G>A (C11orf65)	XP_005271471.1:n.*38+1311G>A
XM_005271415.4:c.804+1311G>A (C11orf65)	XP_005271472.1:n.804+1311G>A
XM_005271562.5:c.7951C>T (ATM)	XP_005271619.2:p.Gln2651Ter
XM_006718843.4:c.7951C>T (ATM)	XP_006718906.1:p.Gln2651Ter
XM_006718845.2:c.3907C>T (ATM)	XP_006718908.1:p.Gln1303Ter
XM_011542840.3:c.7951C>T (ATM)	XP_011541142.1:p.Gln2651Ter
XM_011542842.3:c.7786C>T (ATM)	XP_011541144.1:p.Gln2596Ter
XM_011542843.2:c.7951C>T (ATM)	XP_011541145.1:p.Gln2651Ter
XM_011542844.3:c.6907C>T (ATM)	XP_011541146.1:p.Gln2303Ter
XM_011542845.2:c.6643C>T (ATM)	XP_011541147.1:p.Gln2215Ter
XM_017017789.2:c.7951C>T (ATM)	XP_016873278.1:p.Gln2651Ter
XM_017017790.2:c.7951C>T (ATM)	XP_016873279.1:p.Gln2651Ter
NM_001330368.2:c.641-24838G>A (C11orf65)	NP_001317297.1:n.641-24838G>A
NM_001351110.2:c.*38+1311G>A (C11orf65)	NP_001338039.1:n.*38+1311G>A
NM_001351834.2:c.7951C>T (ATM)	NP_001338763.1:p.Gln2651Ter
NM_000051.4:c.7951C>T (ATM) MANE Select	NP_000042.3:p.Gln2651Ter
NR_147053.3:n.2372+1311G>A (C11orf65)