Canonical Allele Identifier: CA10579252

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 231314
• ClinVar RCV Id: RCV000218804 ; RCV002518301
• dbSNP Id: rs876659083
• gnomAD v4: 11-108329106-G-A
• MyVariant Identifiers: chr11:g.108199833G>A (hg19) ; chr11:g.108329106G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108329106G>A , CM000673.2:g.108329106G>A	GRCh38
NC_000011.9:g.108199833G>A , CM000673.1:g.108199833G>A	GRCh37
NC_000011.8:g.107705043G>A	NCBI36
NG_009830.1:g.111275G>A , LRG_135:g.111275G>A
NG_054724.1:g.145727C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7175G>A (ATM)	ENSP00000388058.2:p.Arg2392Gln
ENST00000713593.1:c.*6646G>A (ATM)	ENSP00000518889.1:n.*6646G>A
ENST00000278616.9:c.7175G>A (ATM)	ENSP00000278616.4:p.Arg2392Gln
ENST00000525056.2:n.1594G>A (ATM)
ENST00000525537.3:n.132G>A (ATM)
ENST00000638786.2:n.12G>A (ATM)
ENST00000682286.1:n.1932G>A (ATM)
ENST00000682302.1:n.1593G>A (ATM)
ENST00000683174.1:n.8659G>A (ATM)
ENST00000683524.1:n.2399G>A (ATM)
ENST00000684152.1:n.2889G>A (ATM)
ENST00000684447.1:n.1638G>A (ATM)
ENST00000527805.6:c.*2239G>A (ATM)	ENSP00000435747.2:n.*2239G>A
ENST00000675595.1:c.*2310G>A (ATM)	ENSP00000502563.1:n.*2310G>A
ENST00000675843.1:c.7175G>A (ATM) MANE Select	ENSP00000501606.1:p.Arg2392Gln
ENST00000278616.8:c.7175G>A (ATM)	ENSP00000278616.4:p.Arg2392Gln
ENST00000452508.6:c.7175G>A (ATM)	ENSP00000388058.2:p.Arg2392Gln
ENST00000524792.5:n.3390G>A (ATM)
ENST00000525537.2:n.451G>A (ATM)
ENST00000525729.5:c.641-20035C>T (C11orf65)	ENSP00000433395.1:n.641-20035C>T
ENST00000527389.2:n.200G>A (ATM)
ENST00000533690.5:n.2579G>A (ATM)
NM_000051.3:c.7175G>A , LRG_135t1:c.7175G>A (ATM)	NP_000042.3:p.Arg2392Gln
XM_005271561.3:c.7175G>A (ATM)	XP_005271618.2:p.Arg2392Gln
XM_005271562.3:c.7175G>A (ATM)	XP_005271619.2:p.Arg2392Gln
XM_006718843.2:c.7175G>A (ATM)	XP_006718906.1:p.Arg2392Gln
XM_006718845.1:c.3131G>A (ATM)	XP_006718908.1:p.Arg1044Gln
XM_011542840.1:c.7175G>A (ATM)	XP_011541142.1:p.Arg2392Gln
XM_011542841.1:c.7175G>A (ATM)	XP_011541143.1:p.Arg2392Gln
XM_011542842.1:c.7010G>A (ATM)	XP_011541144.1:p.Arg2337Gln
XM_011542843.1:c.7175G>A (ATM)	XP_011541145.1:p.Arg2392Gln
XM_011542844.1:c.6131G>A (ATM)	XP_011541146.1:p.Arg2044Gln
XM_011542845.1:c.5867G>A (ATM)	XP_011541147.1:p.Arg1956Gln
XM_011542847.1:c.2246G>A (ATM)	XP_011541149.1:p.Arg749Gln
NM_001330368.1:c.641-20035C>T (C11orf65)	NP_001317297.1:n.641-20035C>T
NM_001351110.1:c.*38+6114C>T (C11orf65)	NP_001338039.1:n.*38+6114C>T
NM_001351834.1:c.7175G>A (ATM)	NP_001338763.1:p.Arg2392Gln
XM_005271562.5:c.7175G>A (ATM)	XP_005271619.2:p.Arg2392Gln
XM_006718843.4:c.7175G>A (ATM)	XP_006718906.1:p.Arg2392Gln
XM_006718845.2:c.3131G>A (ATM)	XP_006718908.1:p.Arg1044Gln
XM_011542840.3:c.7175G>A (ATM)	XP_011541142.1:p.Arg2392Gln
XM_011542842.3:c.7010G>A (ATM)	XP_011541144.1:p.Arg2337Gln
XM_011542843.2:c.7175G>A (ATM)	XP_011541145.1:p.Arg2392Gln
XM_011542844.3:c.6131G>A (ATM)	XP_011541146.1:p.Arg2044Gln
XM_011542845.2:c.5867G>A (ATM)	XP_011541147.1:p.Arg1956Gln
XM_017017789.2:c.7175G>A (ATM)	XP_016873278.1:p.Arg2392Gln
XM_017017790.2:c.7175G>A (ATM)	XP_016873279.1:p.Arg2392Gln
NM_001330368.2:c.641-20035C>T (C11orf65)	NP_001317297.1:n.641-20035C>T
NM_001351110.2:c.*38+6114C>T (C11orf65)	NP_001338039.1:n.*38+6114C>T
NM_001351834.2:c.7175G>A (ATM)	NP_001338763.1:p.Arg2392Gln
NM_000051.4:c.7175G>A (ATM) MANE Select	NP_000042.3:p.Arg2392Gln