Canonical Allele Identifier: CA192266

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 185555
• ClinVar RCV Id: RCV000164998 ; RCV000470464 ; RCV001697122
• dbSNP Id: rs770552705
• ExAC: 11:108206619 G / A
• gnomAD v2: 11-108206619-G-A
• gnomAD v3: 11-108335892-G-A
• gnomAD v4: 11-108335892-G-A
• MyVariant Identifiers: chr11:g.108206619G>A (hg19) ; chr11:g.108335892G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108335892G>A , CM000673.2:g.108335892G>A	GRCh38
NC_000011.9:g.108206619G>A , CM000673.1:g.108206619G>A	GRCh37
NC_000011.8:g.107711829G>A	NCBI36
NG_009830.1:g.118061G>A , LRG_135:g.118061G>A
NG_054724.1:g.138941C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.8199G>A (ATM)	ENSP00000388058.2:p.Gln2733=
ENST00000713593.1:c.*7670G>A (ATM)	ENSP00000518889.1:n.*7670G>A
ENST00000278616.9:c.8199G>A (ATM)	ENSP00000278616.4:p.Gln2733=
ENST00000525056.2:n.2618G>A (ATM)
ENST00000638786.2:n.897G>A (ATM)
ENST00000682286.1:n.2956G>A (ATM)
ENST00000682302.1:n.2617G>A (ATM)
ENST00000683174.1:n.9683G>A (ATM)
ENST00000683524.1:n.3423G>A (ATM)
ENST00000684152.1:n.3615G>A (ATM)
ENST00000684180.1:n.673G>A (ATM)
ENST00000684447.1:n.4692G>A (ATM)
ENST00000527805.6:c.*3263G>A (ATM)	ENSP00000435747.2:n.*3263G>A
ENST00000675595.1:c.*3334G>A (ATM)	ENSP00000502563.1:n.*3334G>A
ENST00000675843.1:c.8199G>A (ATM) MANE Select	ENSP00000501606.1:p.Gln2733=
ENST00000278616.8:c.8199G>A (ATM)	ENSP00000278616.4:p.Gln2733=
ENST00000452508.6:c.8199G>A (ATM)	ENSP00000388058.2:p.Gln2733=
ENST00000524755.5:c.227-600C>T (C11orf65)
ENST00000524792.5:n.4414G>A (ATM)
ENST00000525056.1:n.396G>A (ATM)
ENST00000525729.5:c.641-26821C>T (C11orf65)	ENSP00000433395.1:n.641-26821C>T
ENST00000527531.5:c.*1197-600C>T (C11orf65)	ENSP00000431706.1:n.*1197-600C>T
ENST00000533979.5:n.411G>A (ATM)
ENST00000615746.4:c.*1197-600C>T (C11orf65)	ENSP00000483537.1:n.*1197-600C>T
NM_000051.3:c.8199G>A , LRG_135t1:c.8199G>A (ATM)	NP_000042.3:p.Gln2733=
XM_005271414.3:c.788-600C>T (C11orf65)	XP_005271471.1:n.788-600C>T
XM_005271415.3:c.732-600C>T (C11orf65)	XP_005271472.1:n.732-600C>T
XM_005271561.3:c.8199G>A (ATM)	XP_005271618.2:p.Gln2733=
XM_005271562.3:c.8199G>A (ATM)	XP_005271619.2:p.Gln2733=
XM_006718843.2:c.8199G>A (ATM)	XP_006718906.1:p.Gln2733=
XM_006718845.1:c.4155G>A (ATM)	XP_006718908.1:p.Gln1385=
XM_011542840.1:c.8199G>A (ATM)	XP_011541142.1:p.Gln2733=
XM_011542841.1:c.8199G>A (ATM)	XP_011541143.1:p.Gln2733=
XM_011542842.1:c.8034G>A (ATM)	XP_011541144.1:p.Gln2678=
XM_011542843.1:c.8199G>A (ATM)	XP_011541145.1:p.Gln2733=
XM_011542844.1:c.7155G>A (ATM)	XP_011541146.1:p.Gln2385=
XM_011542845.1:c.6891G>A (ATM)	XP_011541147.1:p.Gln2297=
XM_011542847.1:c.3270G>A (ATM)	XP_011541149.1:p.Gln1090=
NM_001330368.1:c.641-26821C>T (C11orf65)	NP_001317297.1:n.641-26821C>T
NM_001351110.1:c.695-600C>T (C11orf65)	NP_001338039.1:n.695-600C>T
NM_001351834.1:c.8199G>A (ATM)	NP_001338763.1:p.Gln2733=
NR_147053.2:n.2302-600C>T (C11orf65)
XM_005271414.4:c.788-600C>T (C11orf65)	XP_005271471.1:n.788-600C>T
XM_005271415.4:c.732-600C>T (C11orf65)	XP_005271472.1:n.732-600C>T
XM_005271562.5:c.8199G>A (ATM)	XP_005271619.2:p.Gln2733=
XM_006718843.4:c.8199G>A (ATM)	XP_006718906.1:p.Gln2733=
XM_006718845.2:c.4155G>A (ATM)	XP_006718908.1:p.Gln1385=
XM_011542840.3:c.8199G>A (ATM)	XP_011541142.1:p.Gln2733=
XM_011542842.3:c.8034G>A (ATM)	XP_011541144.1:p.Gln2678=
XM_011542843.2:c.8199G>A (ATM)	XP_011541145.1:p.Gln2733=
XM_011542844.3:c.7155G>A (ATM)	XP_011541146.1:p.Gln2385=
XM_011542845.2:c.6891G>A (ATM)	XP_011541147.1:p.Gln2297=
XM_017017789.2:c.8199G>A (ATM)	XP_016873278.1:p.Gln2733=
XM_017017790.2:c.8199G>A (ATM)	XP_016873279.1:p.Gln2733=
NM_001330368.2:c.641-26821C>T (C11orf65)	NP_001317297.1:n.641-26821C>T
NM_001351110.2:c.695-600C>T (C11orf65)	NP_001338039.1:n.695-600C>T
NM_001351834.2:c.8199G>A (ATM)	NP_001338763.1:p.Gln2733=
NM_000051.4:c.8199G>A (ATM) MANE Select	NP_000042.3:p.Gln2733=
NR_147053.3:n.2300-600C>T (C11orf65)