Canonical Allele Identifier: CA382562245

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 919936
• ClinVar RCV Id: RCV001178413
• dbSNP Id: rs1591192429
• MyVariant Identifiers: chr11:g.108205828C>A (hg19) ; chr11:g.108335101C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108335101C>A , CM000673.2:g.108335101C>A	GRCh38
NC_000011.9:g.108205828C>A , CM000673.1:g.108205828C>A	GRCh37
NC_000011.8:g.107711038C>A	NCBI36
NG_009830.1:g.117270C>A , LRG_135:g.117270C>A
NG_054724.1:g.139732G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8143C>A (ATM)	ENSP00000388058.2:p.Leu2715Ile
ENST00000713593.1:c.*7614C>A (ATM)	ENSP00000518889.1:n.*7614C>A
ENST00000278616.9:c.8143C>A (ATM)	ENSP00000278616.4:p.Leu2715Ile
ENST00000525056.2:n.2562C>A (ATM)
ENST00000638786.2:n.841C>A (ATM)
ENST00000682286.1:n.2900C>A (ATM)
ENST00000682302.1:n.2561C>A (ATM)
ENST00000683174.1:n.9627C>A (ATM)
ENST00000683524.1:n.3367C>A (ATM)
ENST00000684152.1:n.3559C>A (ATM)
ENST00000684180.1:n.617C>A (ATM)
ENST00000684447.1:n.4636C>A (ATM)
ENST00000527805.6:c.*3207C>A (ATM)	ENSP00000435747.2:n.*3207C>A
ENST00000675595.1:c.*3278C>A (ATM)	ENSP00000502563.1:n.*3278C>A
ENST00000675843.1:c.8143C>A (ATM) MANE Select	ENSP00000501606.1:p.Leu2715Ile
ENST00000278616.8:c.8143C>A (ATM)	ENSP00000278616.4:p.Leu2715Ile
ENST00000452508.6:c.8143C>A (ATM)	ENSP00000388058.2:p.Leu2715Ile
ENST00000524755.5:c.299+119G>T (C11orf65)
ENST00000524792.5:n.4358C>A (ATM)
ENST00000525056.1:n.340C>A (ATM)
ENST00000525729.5:c.641-26030G>T (C11orf65)	ENSP00000433395.1:n.641-26030G>T
ENST00000527531.5:c.*1269+119G>T (C11orf65)	ENSP00000431706.1:n.*1269+119G>T
ENST00000533979.5:n.355C>A (ATM)
ENST00000615746.4:c.*1269+119G>T (C11orf65)	ENSP00000483537.1:n.*1269+119G>T
NM_000051.3:c.8143C>A , LRG_135t1:c.8143C>A (ATM)	NP_000042.3:p.Leu2715Ile
XM_005271414.3:c.*38+119G>T (C11orf65)	XP_005271471.1:n.*38+119G>T
XM_005271415.3:c.804+119G>T (C11orf65)	XP_005271472.1:n.804+119G>T
XM_005271561.3:c.8143C>A (ATM)	XP_005271618.2:p.Leu2715Ile
XM_005271562.3:c.8143C>A (ATM)	XP_005271619.2:p.Leu2715Ile
XM_006718843.2:c.8143C>A (ATM)	XP_006718906.1:p.Leu2715Ile
XM_006718845.1:c.4099C>A (ATM)	XP_006718908.1:p.Leu1367Ile
XM_011542840.1:c.8143C>A (ATM)	XP_011541142.1:p.Leu2715Ile
XM_011542841.1:c.8143C>A (ATM)	XP_011541143.1:p.Leu2715Ile
XM_011542842.1:c.7978C>A (ATM)	XP_011541144.1:p.Leu2660Ile
XM_011542843.1:c.8143C>A (ATM)	XP_011541145.1:p.Leu2715Ile
XM_011542844.1:c.7099C>A (ATM)	XP_011541146.1:p.Leu2367Ile
XM_011542845.1:c.6835C>A (ATM)	XP_011541147.1:p.Leu2279Ile
XM_011542847.1:c.3214C>A (ATM)	XP_011541149.1:p.Leu1072Ile
NM_001330368.1:c.641-26030G>T (C11orf65)	NP_001317297.1:n.641-26030G>T
NM_001351110.1:c.*38+119G>T (C11orf65)	NP_001338039.1:n.*38+119G>T
NM_001351834.1:c.8143C>A (ATM)	NP_001338763.1:p.Leu2715Ile
NR_147053.2:n.2374+119G>T (C11orf65)
XM_005271414.4:c.*38+119G>T (C11orf65)	XP_005271471.1:n.*38+119G>T
XM_005271415.4:c.804+119G>T (C11orf65)	XP_005271472.1:n.804+119G>T
XM_005271562.5:c.8143C>A (ATM)	XP_005271619.2:p.Leu2715Ile
XM_006718843.4:c.8143C>A (ATM)	XP_006718906.1:p.Leu2715Ile
XM_006718845.2:c.4099C>A (ATM)	XP_006718908.1:p.Leu1367Ile
XM_011542840.3:c.8143C>A (ATM)	XP_011541142.1:p.Leu2715Ile
XM_011542842.3:c.7978C>A (ATM)	XP_011541144.1:p.Leu2660Ile
XM_011542843.2:c.8143C>A (ATM)	XP_011541145.1:p.Leu2715Ile
XM_011542844.3:c.7099C>A (ATM)	XP_011541146.1:p.Leu2367Ile
XM_011542845.2:c.6835C>A (ATM)	XP_011541147.1:p.Leu2279Ile
XM_017017789.2:c.8143C>A (ATM)	XP_016873278.1:p.Leu2715Ile
XM_017017790.2:c.8143C>A (ATM)	XP_016873279.1:p.Leu2715Ile
NM_001330368.2:c.641-26030G>T (C11orf65)	NP_001317297.1:n.641-26030G>T
NM_001351110.2:c.*38+119G>T (C11orf65)	NP_001338039.1:n.*38+119G>T
NM_001351834.2:c.8143C>A (ATM)	NP_001338763.1:p.Leu2715Ile
NM_000051.4:c.8143C>A (ATM) MANE Select	NP_000042.3:p.Leu2715Ile
NR_147053.3:n.2372+119G>T (C11orf65)