Canonical Allele Identifier: CA891842780

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 570368
• ClinVar RCV Id: RCV000691218
• dbSNP Id: rs1565543844
• MyVariant Identifiers: chr11:g.108206669dup (hg19) ; chr11:g.108335942dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108335942dup , CM000673.2:g.108335942dup	GRCh38
NC_000011.9:g.108206669dup , CM000673.1:g.108206669dup	GRCh37
NC_000011.8:g.107711879dup	NCBI36
NG_009830.1:g.118111dup , LRG_135:g.118111dup
NG_054724.1:g.138892dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8249dup (ATM)	ENSP00000388058.2:p.Leu2750PhefsTer7
ENST00000713593.1:c.*7720dup (ATM)	ENSP00000518889.1:n.*7720dup
ENST00000278616.9:c.8249dup (ATM)	ENSP00000278616.4:p.Leu2750PhefsTer7
ENST00000525056.2:n.2668dup (ATM)
ENST00000638786.2:n.947dup (ATM)
ENST00000682286.1:n.3006dup (ATM)
ENST00000682302.1:n.2667dup (ATM)
ENST00000683174.1:n.9733dup (ATM)
ENST00000683524.1:n.3473dup (ATM)
ENST00000684152.1:n.3665dup (ATM)
ENST00000684180.1:n.723dup (ATM)
ENST00000684447.1:n.4742dup (ATM)
ENST00000527805.6:c.*3313dup (ATM)	ENSP00000435747.2:n.*3313dup
ENST00000675595.1:c.*3384dup (ATM)	ENSP00000502563.1:n.*3384dup
ENST00000675843.1:c.8249dup (ATM) MANE Select	ENSP00000501606.1:p.Leu2750PhefsTer7
ENST00000278616.8:c.8249dup (ATM)	ENSP00000278616.4:p.Leu2750PhefsTer7
ENST00000452508.6:c.8249dup (ATM)	ENSP00000388058.2:p.Leu2750PhefsTer7
ENST00000524755.5:c.227-649dup (C11orf65)
ENST00000524792.5:n.4464dup (ATM)
ENST00000525056.1:n.446dup (ATM)
ENST00000525729.5:c.641-26870dup (C11orf65)	ENSP00000433395.1:n.641-26870dup
ENST00000527531.5:c.*1197-649dup (C11orf65)	ENSP00000431706.1:n.*1197-649dup
ENST00000533979.5:n.461dup (ATM)
ENST00000615746.4:c.*1197-649dup (C11orf65)	ENSP00000483537.1:n.*1197-649dup
NM_000051.3:c.8249dup , LRG_135t1:c.8249dup (ATM)	NP_000042.3:p.Leu2750PhefsTer7
XM_005271414.3:c.788-649dup (C11orf65)	XP_005271471.1:n.788-649dup
XM_005271415.3:c.732-649dup (C11orf65)	XP_005271472.1:n.732-649dup
XM_005271561.3:c.8249dup (ATM)	XP_005271618.2:p.Leu2750PhefsTer7
XM_005271562.3:c.8249dup (ATM)	XP_005271619.2:p.Leu2750PhefsTer7
XM_006718843.2:c.8249dup (ATM)	XP_006718906.1:p.Leu2750PhefsTer7
XM_006718845.1:c.4205dup (ATM)	XP_006718908.1:p.Leu1402PhefsTer7
XM_011542840.1:c.8249dup (ATM)	XP_011541142.1:p.Leu2750PhefsTer7
XM_011542841.1:c.8249dup (ATM)	XP_011541143.1:p.Leu2750PhefsTer7
XM_011542842.1:c.8084dup (ATM)	XP_011541144.1:p.Leu2695PhefsTer7
XM_011542843.1:c.8249dup (ATM)	XP_011541145.1:p.Leu2750PhefsTer7
XM_011542844.1:c.7205dup (ATM)	XP_011541146.1:p.Leu2402PhefsTer7
XM_011542845.1:c.6941dup (ATM)	XP_011541147.1:p.Leu2314PhefsTer7
XM_011542847.1:c.3320dup (ATM)	XP_011541149.1:p.Leu1107PhefsTer7
NM_001330368.1:c.641-26870dup (C11orf65)	NP_001317297.1:n.641-26870dup
NM_001351110.1:c.695-649dup (C11orf65)	NP_001338039.1:n.695-649dup
NM_001351834.1:c.8249dup (ATM)	NP_001338763.1:p.Leu2750PhefsTer7
NR_147053.2:n.2302-649dup (C11orf65)
XM_005271414.4:c.788-649dup (C11orf65)	XP_005271471.1:n.788-649dup
XM_005271415.4:c.732-649dup (C11orf65)	XP_005271472.1:n.732-649dup
XM_005271562.5:c.8249dup (ATM)	XP_005271619.2:p.Leu2750PhefsTer7
XM_006718843.4:c.8249dup (ATM)	XP_006718906.1:p.Leu2750PhefsTer7
XM_006718845.2:c.4205dup (ATM)	XP_006718908.1:p.Leu1402PhefsTer7
XM_011542840.3:c.8249dup (ATM)	XP_011541142.1:p.Leu2750PhefsTer7
XM_011542842.3:c.8084dup (ATM)	XP_011541144.1:p.Leu2695PhefsTer7
XM_011542843.2:c.8249dup (ATM)	XP_011541145.1:p.Leu2750PhefsTer7
XM_011542844.3:c.7205dup (ATM)	XP_011541146.1:p.Leu2402PhefsTer7
XM_011542845.2:c.6941dup (ATM)	XP_011541147.1:p.Leu2314PhefsTer7
XM_017017789.2:c.8249dup (ATM)	XP_016873278.1:p.Leu2750PhefsTer7
XM_017017790.2:c.8249dup (ATM)	XP_016873279.1:p.Leu2750PhefsTer7
NM_001330368.2:c.641-26870dup (C11orf65)	NP_001317297.1:n.641-26870dup
NM_001351110.2:c.695-649dup (C11orf65)	NP_001338039.1:n.695-649dup
NM_001351834.2:c.8249dup (ATM)	NP_001338763.1:p.Leu2750PhefsTer7
NM_000051.4:c.8249dup (ATM) MANE Select	NP_000042.3:p.Leu2750PhefsTer7
NR_147053.3:n.2300-649dup (C11orf65)