Canonical Allele Identifier: CA16613495

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 407608
• ClinVar RCV Id: RCV000472748
• dbSNP Id: rs989577687
• MyVariant Identifiers: chr11:g.108205771G>A (hg19) ; chr11:g.108335044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108335044G>A , CM000673.2:g.108335044G>A	GRCh38
NC_000011.9:g.108205771G>A , CM000673.1:g.108205771G>A	GRCh37
NC_000011.8:g.107710981G>A	NCBI36
NG_009830.1:g.117213G>A , LRG_135:g.117213G>A
NG_054724.1:g.139789C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8086G>A (ATM)	ENSP00000388058.2:p.Val2696Ile
ENST00000713593.1:c.*7557G>A (ATM)	ENSP00000518889.1:n.*7557G>A
ENST00000278616.9:c.8086G>A (ATM)	ENSP00000278616.4:p.Val2696Ile
ENST00000525056.2:n.2505G>A (ATM)
ENST00000638786.2:n.784G>A (ATM)
ENST00000682286.1:n.2843G>A (ATM)
ENST00000682302.1:n.2504G>A (ATM)
ENST00000683174.1:n.9570G>A (ATM)
ENST00000683524.1:n.3310G>A (ATM)
ENST00000684152.1:n.3502G>A (ATM)
ENST00000684180.1:n.560G>A (ATM)
ENST00000684447.1:n.4579G>A (ATM)
ENST00000527805.6:c.*3150G>A (ATM)	ENSP00000435747.2:n.*3150G>A
ENST00000675595.1:c.*3221G>A (ATM)	ENSP00000502563.1:n.*3221G>A
ENST00000675843.1:c.8086G>A (ATM) MANE Select	ENSP00000501606.1:p.Val2696Ile
ENST00000278616.8:c.8086G>A (ATM)	ENSP00000278616.4:p.Val2696Ile
ENST00000452508.6:c.8086G>A (ATM)	ENSP00000388058.2:p.Val2696Ile
ENST00000524755.5:c.299+176C>T (C11orf65)
ENST00000524792.5:n.4301G>A (ATM)
ENST00000525056.1:n.283G>A (ATM)
ENST00000525729.5:c.641-25973C>T (C11orf65)	ENSP00000433395.1:n.641-25973C>T
ENST00000527531.5:c.*1269+176C>T (C11orf65)	ENSP00000431706.1:n.*1269+176C>T
ENST00000533979.5:n.298G>A (ATM)
ENST00000615746.4:c.*1269+176C>T (C11orf65)	ENSP00000483537.1:n.*1269+176C>T
NM_000051.3:c.8086G>A , LRG_135t1:c.8086G>A (ATM)	NP_000042.3:p.Val2696Ile
XM_005271414.3:c.*38+176C>T (C11orf65)	XP_005271471.1:n.*38+176C>T
XM_005271415.3:c.804+176C>T (C11orf65)	XP_005271472.1:n.804+176C>T
XM_005271561.3:c.8086G>A (ATM)	XP_005271618.2:p.Val2696Ile
XM_005271562.3:c.8086G>A (ATM)	XP_005271619.2:p.Val2696Ile
XM_006718843.2:c.8086G>A (ATM)	XP_006718906.1:p.Val2696Ile
XM_006718845.1:c.4042G>A (ATM)	XP_006718908.1:p.Val1348Ile
XM_011542840.1:c.8086G>A (ATM)	XP_011541142.1:p.Val2696Ile
XM_011542841.1:c.8086G>A (ATM)	XP_011541143.1:p.Val2696Ile
XM_011542842.1:c.7921G>A (ATM)	XP_011541144.1:p.Val2641Ile
XM_011542843.1:c.8086G>A (ATM)	XP_011541145.1:p.Val2696Ile
XM_011542844.1:c.7042G>A (ATM)	XP_011541146.1:p.Val2348Ile
XM_011542845.1:c.6778G>A (ATM)	XP_011541147.1:p.Val2260Ile
XM_011542847.1:c.3157G>A (ATM)	XP_011541149.1:p.Val1053Ile
NM_001330368.1:c.641-25973C>T (C11orf65)	NP_001317297.1:n.641-25973C>T
NM_001351110.1:c.*38+176C>T (C11orf65)	NP_001338039.1:n.*38+176C>T
NM_001351834.1:c.8086G>A (ATM)	NP_001338763.1:p.Val2696Ile
NR_147053.2:n.2374+176C>T (C11orf65)
XM_005271414.4:c.*38+176C>T (C11orf65)	XP_005271471.1:n.*38+176C>T
XM_005271415.4:c.804+176C>T (C11orf65)	XP_005271472.1:n.804+176C>T
XM_005271562.5:c.8086G>A (ATM)	XP_005271619.2:p.Val2696Ile
XM_006718843.4:c.8086G>A (ATM)	XP_006718906.1:p.Val2696Ile
XM_006718845.2:c.4042G>A (ATM)	XP_006718908.1:p.Val1348Ile
XM_011542840.3:c.8086G>A (ATM)	XP_011541142.1:p.Val2696Ile
XM_011542842.3:c.7921G>A (ATM)	XP_011541144.1:p.Val2641Ile
XM_011542843.2:c.8086G>A (ATM)	XP_011541145.1:p.Val2696Ile
XM_011542844.3:c.7042G>A (ATM)	XP_011541146.1:p.Val2348Ile
XM_011542845.2:c.6778G>A (ATM)	XP_011541147.1:p.Val2260Ile
XM_017017789.2:c.8086G>A (ATM)	XP_016873278.1:p.Val2696Ile
XM_017017790.2:c.8086G>A (ATM)	XP_016873279.1:p.Val2696Ile
NM_001330368.2:c.641-25973C>T (C11orf65)	NP_001317297.1:n.641-25973C>T
NM_001351110.2:c.*38+176C>T (C11orf65)	NP_001338039.1:n.*38+176C>T
NM_001351834.2:c.8086G>A (ATM)	NP_001338763.1:p.Val2696Ile
NM_000051.4:c.8086G>A (ATM) MANE Select	NP_000042.3:p.Val2696Ile
NR_147053.3:n.2372+176C>T (C11orf65)