Canonical Allele Identifier: CA10579276

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 234050
• ClinVar RCV Id: RCV000221138 ; RCV003469096 ; RCV002516176
• dbSNP Id: rs587781897
• gnomAD v2: 11-108204615-G-A
• gnomAD v4: 11-108333888-G-A
• MyVariant Identifiers: chr11:g.108204615G>A (hg19) ; chr11:g.108333888G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108333888G>A , CM000673.2:g.108333888G>A	GRCh38
NC_000011.9:g.108204615G>A , CM000673.1:g.108204615G>A	GRCh37
NC_000011.8:g.107709825G>A	NCBI36
NG_009830.1:g.116057G>A , LRG_135:g.116057G>A
NG_054724.1:g.140945C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7930G>A (ATM)	ENSP00000388058.2:p.Gly2644Ser
ENST00000713593.1:c.*7401G>A (ATM)	ENSP00000518889.1:n.*7401G>A
ENST00000278616.9:c.7930G>A (ATM)	ENSP00000278616.4:p.Gly2644Ser
ENST00000525056.2:n.2349G>A (ATM)
ENST00000638786.2:n.628G>A (ATM)
ENST00000682286.1:n.2687G>A (ATM)
ENST00000682302.1:n.2348G>A (ATM)
ENST00000683174.1:n.9414G>A (ATM)
ENST00000683524.1:n.3154G>A (ATM)
ENST00000684152.1:n.3346G>A (ATM)
ENST00000684180.1:n.404G>A (ATM)
ENST00000684447.1:n.4423G>A (ATM)
ENST00000527805.6:c.*2994G>A (ATM)	ENSP00000435747.2:n.*2994G>A
ENST00000675595.1:c.*3065G>A (ATM)	ENSP00000502563.1:n.*3065G>A
ENST00000675843.1:c.7930G>A (ATM) MANE Select	ENSP00000501606.1:p.Gly2644Ser
ENST00000278616.8:c.7930G>A (ATM)	ENSP00000278616.4:p.Gly2644Ser
ENST00000452508.6:c.7930G>A (ATM)	ENSP00000388058.2:p.Gly2644Ser
ENST00000524755.5:c.299+1332C>T (C11orf65)
ENST00000524792.5:n.4145G>A (ATM)
ENST00000525056.1:n.127G>A (ATM)
ENST00000525729.5:c.641-24817C>T (C11orf65)	ENSP00000433395.1:n.641-24817C>T
ENST00000527531.5:c.*1269+1332C>T (C11orf65)	ENSP00000431706.1:n.*1269+1332C>T
ENST00000533690.5:n.3334G>A (ATM)
ENST00000533979.5:n.142G>A (ATM)
ENST00000615746.4:c.*1269+1332C>T (C11orf65)	ENSP00000483537.1:n.*1269+1332C>T
NM_000051.3:c.7930G>A , LRG_135t1:c.7930G>A (ATM)	NP_000042.3:p.Gly2644Ser
XM_005271414.3:c.*38+1332C>T (C11orf65)	XP_005271471.1:n.*38+1332C>T
XM_005271415.3:c.804+1332C>T (C11orf65)	XP_005271472.1:n.804+1332C>T
XM_005271561.3:c.7930G>A (ATM)	XP_005271618.2:p.Gly2644Ser
XM_005271562.3:c.7930G>A (ATM)	XP_005271619.2:p.Gly2644Ser
XM_006718843.2:c.7930G>A (ATM)	XP_006718906.1:p.Gly2644Ser
XM_006718845.1:c.3886G>A (ATM)	XP_006718908.1:p.Gly1296Ser
XM_011542840.1:c.7930G>A (ATM)	XP_011541142.1:p.Gly2644Ser
XM_011542841.1:c.7930G>A (ATM)	XP_011541143.1:p.Gly2644Ser
XM_011542842.1:c.7765G>A (ATM)	XP_011541144.1:p.Gly2589Ser
XM_011542843.1:c.7930G>A (ATM)	XP_011541145.1:p.Gly2644Ser
XM_011542844.1:c.6886G>A (ATM)	XP_011541146.1:p.Gly2296Ser
XM_011542845.1:c.6622G>A (ATM)	XP_011541147.1:p.Gly2208Ser
XM_011542847.1:c.3001G>A (ATM)	XP_011541149.1:p.Gly1001Ser
NM_001330368.1:c.641-24817C>T (C11orf65)	NP_001317297.1:n.641-24817C>T
NM_001351110.1:c.*38+1332C>T (C11orf65)	NP_001338039.1:n.*38+1332C>T
NM_001351834.1:c.7930G>A (ATM)	NP_001338763.1:p.Gly2644Ser
NR_147053.2:n.2374+1332C>T (C11orf65)
XM_005271414.4:c.*38+1332C>T (C11orf65)	XP_005271471.1:n.*38+1332C>T
XM_005271415.4:c.804+1332C>T (C11orf65)	XP_005271472.1:n.804+1332C>T
XM_005271562.5:c.7930G>A (ATM)	XP_005271619.2:p.Gly2644Ser
XM_006718843.4:c.7930G>A (ATM)	XP_006718906.1:p.Gly2644Ser
XM_006718845.2:c.3886G>A (ATM)	XP_006718908.1:p.Gly1296Ser
XM_011542840.3:c.7930G>A (ATM)	XP_011541142.1:p.Gly2644Ser
XM_011542842.3:c.7765G>A (ATM)	XP_011541144.1:p.Gly2589Ser
XM_011542843.2:c.7930G>A (ATM)	XP_011541145.1:p.Gly2644Ser
XM_011542844.3:c.6886G>A (ATM)	XP_011541146.1:p.Gly2296Ser
XM_011542845.2:c.6622G>A (ATM)	XP_011541147.1:p.Gly2208Ser
XM_017017789.2:c.7930G>A (ATM)	XP_016873278.1:p.Gly2644Ser
XM_017017790.2:c.7930G>A (ATM)	XP_016873279.1:p.Gly2644Ser
NM_001330368.2:c.641-24817C>T (C11orf65)	NP_001317297.1:n.641-24817C>T
NM_001351110.2:c.*38+1332C>T (C11orf65)	NP_001338039.1:n.*38+1332C>T
NM_001351834.2:c.7930G>A (ATM)	NP_001338763.1:p.Gly2644Ser
NM_000051.4:c.7930G>A (ATM) MANE Select	NP_000042.3:p.Gly2644Ser
NR_147053.3:n.2372+1332C>T (C11orf65)