Canonical Allele Identifier: CA382561017

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 2704949
• ClinVar RCV Id: RCV003501174
• dbSNP Id: rs775295535
• MyVariant Identifiers: chr11:g.108202667C>T (hg19) ; chr11:g.108331940C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108331940C>T , CM000673.2:g.108331940C>T	GRCh38
NC_000011.9:g.108202667C>T , CM000673.1:g.108202667C>T	GRCh37
NC_000011.8:g.107707877C>T	NCBI36
NG_009830.1:g.114109C>T , LRG_135:g.114109C>T
NG_054724.1:g.142893G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.7691C>T (ATM)	ENSP00000388058.2:p.Ala2564Val
ENST00000713593.1:c.*7162C>T (ATM)	ENSP00000518889.1:n.*7162C>T
ENST00000278616.9:c.7691C>T (ATM)	ENSP00000278616.4:p.Ala2564Val
ENST00000525056.2:n.2110C>T (ATM)
ENST00000525537.3:n.648C>T (ATM)
ENST00000638786.2:n.528C>T (ATM)
ENST00000682286.1:n.2448C>T (ATM)
ENST00000682302.1:n.2109C>T (ATM)
ENST00000683174.1:n.9175C>T (ATM)
ENST00000683524.1:n.2915C>T (ATM)
ENST00000684152.1:n.3343+383C>T (ATM)
ENST00000684447.1:n.2475C>T (ATM)
ENST00000527805.6:c.*2755C>T (ATM)	ENSP00000435747.2:n.*2755C>T
ENST00000675595.1:c.*2826C>T (ATM)	ENSP00000502563.1:n.*2826C>T
ENST00000675843.1:c.7691C>T (ATM) MANE Select	ENSP00000501606.1:p.Ala2564Val
ENST00000278616.8:c.7691C>T (ATM)	ENSP00000278616.4:p.Ala2564Val
ENST00000452508.6:c.7691C>T (ATM)	ENSP00000388058.2:p.Ala2564Val
ENST00000524755.5:c.300-373G>A (C11orf65)
ENST00000524792.5:n.3906C>T (ATM)
ENST00000525729.5:c.641-22869G>A (C11orf65)	ENSP00000433395.1:n.641-22869G>A
ENST00000527531.5:c.*1270-373G>A (C11orf65)	ENSP00000431706.1:n.*1270-373G>A
ENST00000533690.5:n.3095C>T (ATM)
ENST00000615746.4:c.*1270-373G>A (C11orf65)	ENSP00000483537.1:n.*1270-373G>A
NM_000051.3:c.7691C>T , LRG_135t1:c.7691C>T (ATM)	NP_000042.3:p.Ala2564Val
XM_005271414.3:c.*39-373G>A (C11orf65)	XP_005271471.1:n.*39-373G>A
XM_005271415.3:c.805-373G>A (C11orf65)	XP_005271472.1:n.805-373G>A
XM_005271561.3:c.7691C>T (ATM)	XP_005271618.2:p.Ala2564Val
XM_005271562.3:c.7691C>T (ATM)	XP_005271619.2:p.Ala2564Val
XM_006718843.2:c.7691C>T (ATM)	XP_006718906.1:p.Ala2564Val
XM_006718845.1:c.3647C>T (ATM)	XP_006718908.1:p.Ala1216Val
XM_011542840.1:c.7691C>T (ATM)	XP_011541142.1:p.Ala2564Val
XM_011542841.1:c.7691C>T (ATM)	XP_011541143.1:p.Ala2564Val
XM_011542842.1:c.7526C>T (ATM)	XP_011541144.1:p.Ala2509Val
XM_011542843.1:c.7691C>T (ATM)	XP_011541145.1:p.Ala2564Val
XM_011542844.1:c.6647C>T (ATM)	XP_011541146.1:p.Ala2216Val
XM_011542845.1:c.6383C>T (ATM)	XP_011541147.1:p.Ala2128Val
XM_011542847.1:c.2762C>T (ATM)	XP_011541149.1:p.Ala921Val
NM_001330368.1:c.641-22869G>A (C11orf65)	NP_001317297.1:n.641-22869G>A
NM_001351110.1:c.*38+3280G>A (C11orf65)	NP_001338039.1:n.*38+3280G>A
NM_001351834.1:c.7691C>T (ATM)	NP_001338763.1:p.Ala2564Val
NR_147053.2:n.2375-373G>A (C11orf65)
XM_005271414.4:c.*39-373G>A (C11orf65)	XP_005271471.1:n.*39-373G>A
XM_005271415.4:c.805-373G>A (C11orf65)	XP_005271472.1:n.805-373G>A
XM_005271562.5:c.7691C>T (ATM)	XP_005271619.2:p.Ala2564Val
XM_006718843.4:c.7691C>T (ATM)	XP_006718906.1:p.Ala2564Val
XM_006718845.2:c.3647C>T (ATM)	XP_006718908.1:p.Ala1216Val
XM_011542840.3:c.7691C>T (ATM)	XP_011541142.1:p.Ala2564Val
XM_011542842.3:c.7526C>T (ATM)	XP_011541144.1:p.Ala2509Val
XM_011542843.2:c.7691C>T (ATM)	XP_011541145.1:p.Ala2564Val
XM_011542844.3:c.6647C>T (ATM)	XP_011541146.1:p.Ala2216Val
XM_011542845.2:c.6383C>T (ATM)	XP_011541147.1:p.Ala2128Val
XM_017017789.2:c.7691C>T (ATM)	XP_016873278.1:p.Ala2564Val
XM_017017790.2:c.7691C>T (ATM)	XP_016873279.1:p.Ala2564Val
NM_001330368.2:c.641-22869G>A (C11orf65)	NP_001317297.1:n.641-22869G>A
NM_001351110.2:c.*38+3280G>A (C11orf65)	NP_001338039.1:n.*38+3280G>A
NM_001351834.2:c.7691C>T (ATM)	NP_001338763.1:p.Ala2564Val
NM_000051.4:c.7691C>T (ATM) MANE Select	NP_000042.3:p.Ala2564Val
NR_147053.3:n.2373-373G>A (C11orf65)