Canonical Allele Identifier: CA382556964

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 1756080
• ClinVar RCV Id: RCV003500738 ; RCV002378067 ; RCV003471359
• MyVariant Identifiers: chr11:g.108196879C>A (hg19) ; chr11:g.108326152C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108326152C>A , CM000673.2:g.108326152C>A	GRCh38
NC_000011.9:g.108196879C>A , CM000673.1:g.108196879C>A	GRCh37
NC_000011.8:g.107702089C>A	NCBI36
NG_009830.1:g.108321C>A , LRG_135:g.108321C>A
NG_054724.1:g.148681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6902C>A (ATM)	ENSP00000388058.2:p.Ala2301Glu
ENST00000713593.1:c.*6373C>A (ATM)	ENSP00000518889.1:n.*6373C>A
ENST00000278616.9:c.6902C>A (ATM)	ENSP00000278616.4:p.Ala2301Glu
ENST00000525056.2:n.1321C>A (ATM)
ENST00000682286.1:n.1659C>A (ATM)
ENST00000682302.1:n.1320C>A (ATM)
ENST00000683174.1:n.8386C>A (ATM)
ENST00000683524.1:n.2126C>A (ATM)
ENST00000684152.1:n.2616C>A (ATM)
ENST00000527805.6:c.*1966C>A (ATM)	ENSP00000435747.2:n.*1966C>A
ENST00000675595.1:c.*2037C>A (ATM)	ENSP00000502563.1:n.*2037C>A
ENST00000675843.1:c.6902C>A (ATM) MANE Select	ENSP00000501606.1:p.Ala2301Glu
ENST00000278616.8:c.6902C>A (ATM)	ENSP00000278616.4:p.Ala2301Glu
ENST00000452508.6:c.6902C>A (ATM)	ENSP00000388058.2:p.Ala2301Glu
ENST00000524792.5:n.3117C>A (ATM)
ENST00000525729.5:c.641-17081G>T (C11orf65)	ENSP00000433395.1:n.641-17081G>T
ENST00000533690.5:n.2306C>A (ATM)
NM_000051.3:c.6902C>A , LRG_135t1:c.6902C>A (ATM)	NP_000042.3:p.Ala2301Glu
XM_005271561.3:c.6902C>A (ATM)	XP_005271618.2:p.Ala2301Glu
XM_005271562.3:c.6902C>A (ATM)	XP_005271619.2:p.Ala2301Glu
XM_006718843.2:c.6902C>A (ATM)	XP_006718906.1:p.Ala2301Glu
XM_006718845.1:c.2858C>A (ATM)	XP_006718908.1:p.Ala953Glu
XM_011542840.1:c.6902C>A (ATM)	XP_011541142.1:p.Ala2301Glu
XM_011542841.1:c.6902C>A (ATM)	XP_011541143.1:p.Ala2301Glu
XM_011542842.1:c.6737C>A (ATM)	XP_011541144.1:p.Ala2246Glu
XM_011542843.1:c.6902C>A (ATM)	XP_011541145.1:p.Ala2301Glu
XM_011542844.1:c.5858C>A (ATM)	XP_011541146.1:p.Ala1953Glu
XM_011542845.1:c.5594C>A (ATM)	XP_011541147.1:p.Ala1865Glu
XM_011542847.1:c.1973C>A (ATM)	XP_011541149.1:p.Ala658Glu
NM_001330368.1:c.641-17081G>T (C11orf65)	NP_001317297.1:n.641-17081G>T
NM_001351110.1:c.*38+9068G>T (C11orf65)	NP_001338039.1:n.*38+9068G>T
NM_001351834.1:c.6902C>A (ATM)	NP_001338763.1:p.Ala2301Glu
XM_005271562.5:c.6902C>A (ATM)	XP_005271619.2:p.Ala2301Glu
XM_006718843.4:c.6902C>A (ATM)	XP_006718906.1:p.Ala2301Glu
XM_006718845.2:c.2858C>A (ATM)	XP_006718908.1:p.Ala953Glu
XM_011542840.3:c.6902C>A (ATM)	XP_011541142.1:p.Ala2301Glu
XM_011542842.3:c.6737C>A (ATM)	XP_011541144.1:p.Ala2246Glu
XM_011542843.2:c.6902C>A (ATM)	XP_011541145.1:p.Ala2301Glu
XM_011542844.3:c.5858C>A (ATM)	XP_011541146.1:p.Ala1953Glu
XM_011542845.2:c.5594C>A (ATM)	XP_011541147.1:p.Ala1865Glu
XM_017017789.2:c.6902C>A (ATM)	XP_016873278.1:p.Ala2301Glu
XM_017017790.2:c.6902C>A (ATM)	XP_016873279.1:p.Ala2301Glu
NM_001330368.2:c.641-17081G>T (C11orf65)	NP_001317297.1:n.641-17081G>T
NM_001351110.2:c.*38+9068G>T (C11orf65)	NP_001338039.1:n.*38+9068G>T
NM_001351834.2:c.6902C>A (ATM)	NP_001338763.1:p.Ala2301Glu
NM_000051.4:c.6902C>A (ATM) MANE Select	NP_000042.3:p.Ala2301Glu