Canonical Allele Identifier: CA382559575

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 957513
• ClinVar RCV Id: RCV001230504
• dbSNP Id: rs2085983049
• COSMIC: COSM3935308 ; COSM3935309
• MyVariant Identifiers: chr11:g.108199841G>A (hg19) ; chr11:g.108329114G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108329114G>A , CM000673.2:g.108329114G>A	GRCh38
NC_000011.9:g.108199841G>A , CM000673.1:g.108199841G>A	GRCh37
NC_000011.8:g.107705051G>A	NCBI36
NG_009830.1:g.111283G>A , LRG_135:g.111283G>A
NG_054724.1:g.145719C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.7183G>A (ATM)	ENSP00000388058.2:p.Asp2395Asn
ENST00000713593.1:c.*6654G>A (ATM)	ENSP00000518889.1:n.*6654G>A
ENST00000278616.9:c.7183G>A (ATM)	ENSP00000278616.4:p.Asp2395Asn
ENST00000525056.2:n.1602G>A (ATM)
ENST00000525537.3:n.140G>A (ATM)
ENST00000638786.2:n.20G>A (ATM)
ENST00000682286.1:n.1940G>A (ATM)
ENST00000682302.1:n.1601G>A (ATM)
ENST00000683174.1:n.8667G>A (ATM)
ENST00000683524.1:n.2407G>A (ATM)
ENST00000684152.1:n.2897G>A (ATM)
ENST00000684447.1:n.1646G>A (ATM)
ENST00000527805.6:c.*2247G>A (ATM)	ENSP00000435747.2:n.*2247G>A
ENST00000675595.1:c.*2318G>A (ATM)	ENSP00000502563.1:n.*2318G>A
ENST00000675843.1:c.7183G>A (ATM) MANE Select	ENSP00000501606.1:p.Asp2395Asn
ENST00000278616.8:c.7183G>A (ATM)	ENSP00000278616.4:p.Asp2395Asn
ENST00000452508.6:c.7183G>A (ATM)	ENSP00000388058.2:p.Asp2395Asn
ENST00000524792.5:n.3398G>A (ATM)
ENST00000525537.2:n.459G>A (ATM)
ENST00000525729.5:c.641-20043C>T (C11orf65)	ENSP00000433395.1:n.641-20043C>T
ENST00000527389.2:n.208G>A (ATM)
ENST00000533690.5:n.2587G>A (ATM)
NM_000051.3:c.7183G>A , LRG_135t1:c.7183G>A (ATM)	NP_000042.3:p.Asp2395Asn
XM_005271561.3:c.7183G>A (ATM)	XP_005271618.2:p.Asp2395Asn
XM_005271562.3:c.7183G>A (ATM)	XP_005271619.2:p.Asp2395Asn
XM_006718843.2:c.7183G>A (ATM)	XP_006718906.1:p.Asp2395Asn
XM_006718845.1:c.3139G>A (ATM)	XP_006718908.1:p.Asp1047Asn
XM_011542840.1:c.7183G>A (ATM)	XP_011541142.1:p.Asp2395Asn
XM_011542841.1:c.7183G>A (ATM)	XP_011541143.1:p.Asp2395Asn
XM_011542842.1:c.7018G>A (ATM)	XP_011541144.1:p.Asp2340Asn
XM_011542843.1:c.7183G>A (ATM)	XP_011541145.1:p.Asp2395Asn
XM_011542844.1:c.6139G>A (ATM)	XP_011541146.1:p.Asp2047Asn
XM_011542845.1:c.5875G>A (ATM)	XP_011541147.1:p.Asp1959Asn
XM_011542847.1:c.2254G>A (ATM)	XP_011541149.1:p.Asp752Asn
NM_001330368.1:c.641-20043C>T (C11orf65)	NP_001317297.1:n.641-20043C>T
NM_001351110.1:c.*38+6106C>T (C11orf65)	NP_001338039.1:n.*38+6106C>T
NM_001351834.1:c.7183G>A (ATM)	NP_001338763.1:p.Asp2395Asn
XM_005271562.5:c.7183G>A (ATM)	XP_005271619.2:p.Asp2395Asn
XM_006718843.4:c.7183G>A (ATM)	XP_006718906.1:p.Asp2395Asn
XM_006718845.2:c.3139G>A (ATM)	XP_006718908.1:p.Asp1047Asn
XM_011542840.3:c.7183G>A (ATM)	XP_011541142.1:p.Asp2395Asn
XM_011542842.3:c.7018G>A (ATM)	XP_011541144.1:p.Asp2340Asn
XM_011542843.2:c.7183G>A (ATM)	XP_011541145.1:p.Asp2395Asn
XM_011542844.3:c.6139G>A (ATM)	XP_011541146.1:p.Asp2047Asn
XM_011542845.2:c.5875G>A (ATM)	XP_011541147.1:p.Asp1959Asn
XM_017017789.2:c.7183G>A (ATM)	XP_016873278.1:p.Asp2395Asn
XM_017017790.2:c.7183G>A (ATM)	XP_016873279.1:p.Asp2395Asn
NM_001330368.2:c.641-20043C>T (C11orf65)	NP_001317297.1:n.641-20043C>T
NM_001351110.2:c.*38+6106C>T (C11orf65)	NP_001338039.1:n.*38+6106C>T
NM_001351834.2:c.7183G>A (ATM)	NP_001338763.1:p.Asp2395Asn
NM_000051.4:c.7183G>A (ATM) MANE Select	NP_000042.3:p.Asp2395Asn