Canonical Allele Identifier: CA382548229

Gene: ATM C11orf65

Linked Data

• MyVariant Identifiers: chr11:g.108179782G>C (hg19) ; chr11:g.108309055G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108309055G>C , CM000673.2:g.108309055G>C	GRCh38
NC_000011.9:g.108179782G>C , CM000673.1:g.108179782G>C	GRCh37
NC_000011.8:g.107684992G>C	NCBI36
NG_009830.1:g.91224G>C , LRG_135:g.91224G>C
NG_054724.1:g.165778C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5762+1071G>C (ATM)	ENSP00000388058.2:n.5762+1071G>C
ENST00000713593.1:c.*5233+1071G>C (ATM)	ENSP00000518889.1:n.*5233+1071G>C
ENST00000278616.9:c.5762+1071G>C (ATM)	ENSP00000278616.4:n.5762+1071G>C
ENST00000525056.2:n.181+1071G>C (ATM)
ENST00000682286.1:n.519+1071G>C (ATM)
ENST00000682302.1:n.180+1071G>C (ATM)
ENST00000683174.1:n.7246+1071G>C (ATM)
ENST00000683524.1:n.986+1071G>C (ATM)
ENST00000684152.1:n.1476+1071G>C (ATM)
ENST00000527805.6:c.*826+1071G>C (ATM)	ENSP00000435747.2:n.*826+1071G>C
ENST00000675595.1:c.*826+1071G>C (ATM)	ENSP00000502563.1:n.*826+1071G>C
ENST00000675843.1:c.5762+1071G>C (ATM) MANE Select	ENSP00000501606.1:n.5762+1071G>C
ENST00000278616.8:c.5762+1071G>C (ATM)	ENSP00000278616.4:n.5762+1071G>C
ENST00000452508.6:c.5762+1071G>C (ATM)	ENSP00000388058.2:n.5762+1071G>C
ENST00000524792.5:n.1977+1071G>C (ATM)
ENST00000525729.5:c.657C>G (C11orf65)	ENSP00000433395.1:p.Ile219Met
ENST00000529588.5:c.187-1105G>C (ATM)
ENST00000532765.1:n.79+985G>C (ATM)
ENST00000533690.5:n.1166+1071G>C (ATM)
NM_000051.3:c.5762+1071G>C , LRG_135t1:c.5762+1071G>C (ATM)	NP_000042.3:n.5762+1071G>C
XM_005271561.3:c.5762+1071G>C (ATM)	XP_005271618.2:n.5762+1071G>C
XM_005271562.3:c.5762+1071G>C (ATM)	XP_005271619.2:n.5762+1071G>C
XM_006718843.2:c.5762+1071G>C (ATM)	XP_006718906.1:n.5762+1071G>C
XM_006718845.1:c.1718+1071G>C (ATM)	XP_006718908.1:n.1718+1071G>C
XM_011542840.1:c.5762+1071G>C (ATM)	XP_011541142.1:n.5762+1071G>C
XM_011542841.1:c.5762+1071G>C (ATM)	XP_011541143.1:n.5762+1071G>C
XM_011542842.1:c.5597+1071G>C (ATM)	XP_011541144.1:n.5597+1071G>C
XM_011542843.1:c.5762+1071G>C (ATM)	XP_011541145.1:n.5762+1071G>C
XM_011542844.1:c.4718+1071G>C (ATM)	XP_011541146.1:n.4718+1071G>C
XM_011542845.1:c.4454+1071G>C (ATM)	XP_011541147.1:n.4454+1071G>C
XM_011542847.1:c.833+1071G>C (ATM)	XP_011541149.1:n.833+1071G>C
NM_001330368.1:c.657C>G (C11orf65)	NP_001317297.1:p.Ile219Met
NM_001351110.1:c.*55C>G (C11orf65)	NP_001338039.1:n.*55C>G
NM_001351834.1:c.5762+1071G>C (ATM)	NP_001338763.1:n.5762+1071G>C
XM_005271562.5:c.5762+1071G>C (ATM)	XP_005271619.2:n.5762+1071G>C
XM_006718843.4:c.5762+1071G>C (ATM)	XP_006718906.1:n.5762+1071G>C
XM_006718845.2:c.1718+1071G>C (ATM)	XP_006718908.1:n.1718+1071G>C
XM_011542840.3:c.5762+1071G>C (ATM)	XP_011541142.1:n.5762+1071G>C
XM_011542842.3:c.5597+1071G>C (ATM)	XP_011541144.1:n.5597+1071G>C
XM_011542843.2:c.5762+1071G>C (ATM)	XP_011541145.1:n.5762+1071G>C
XM_011542844.3:c.4718+1071G>C (ATM)	XP_011541146.1:n.4718+1071G>C
XM_011542845.2:c.4454+1071G>C (ATM)	XP_011541147.1:n.4454+1071G>C
XM_017017789.2:c.5762+1071G>C (ATM)	XP_016873278.1:n.5762+1071G>C
XM_017017790.2:c.5762+1071G>C (ATM)	XP_016873279.1:n.5762+1071G>C
XM_017017791.1:c.5762+1071G>C (ATM)	XP_016873280.1:n.5762+1071G>C
XR_002957150.1:n.6362+1071G>C (ATM)
NM_001330368.2:c.657C>G (C11orf65)	NP_001317297.1:p.Ile219Met
NM_001351110.2:c.*55C>G (C11orf65)	NP_001338039.1:n.*55C>G
NM_001351834.2:c.5762+1071G>C (ATM)	NP_001338763.1:n.5762+1071G>C
NM_000051.4:c.5762+1071G>C (ATM) MANE Select	NP_000042.3:n.5762+1071G>C