Canonical Allele Identifier: CA10588499

Gene: ATM

Linked Data

• ClinVar Variation Id: 265342
• ClinVar RCV Id: RCV000255794 ; RCV000564660
• dbSNP Id: rs886039488
• MyVariant Identifiers: chr11:g.108158417_108158418del (hg19) ; chr11:g.108287690_108287691del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108287690_108287691del , CM000673.2:g.108287690_108287691del	GRCh38
NC_000011.9:g.108158417_108158418del , CM000673.1:g.108158417_108158418del	GRCh37
NC_000011.8:g.107663627_107663628del	NCBI36
NG_009830.1:g.69859_69860del , LRG_135:g.69859_69860del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4084_4085del	ENSP00000388058.2:p.Ser1362HisfsTer2
ENST00000713593.1:c.*3555_*3556del	ENSP00000518889.1:n.*3555_*3556del
ENST00000278616.9:c.4084_4085del	ENSP00000278616.4:p.Ser1362HisfsTer2
ENST00000533733.6:n.1347_1348del
ENST00000683174.1:n.4234_4235del
ENST00000527805.6:c.4084_4085del	ENSP00000435747.2:p.Ser1362HisfsTer2
ENST00000675595.1:c.3919_3920del	ENSP00000502563.1:p.Ser1307HisfsTer2
ENST00000675843.1:c.4084_4085del MANE Select	ENSP00000501606.1:p.Ser1362HisfsTer2
ENST00000278616.8:c.4084_4085del	ENSP00000278616.4:p.Ser1362HisfsTer2
ENST00000452508.6:c.4084_4085del	ENSP00000388058.2:p.Ser1362HisfsTer2
ENST00000524792.5:n.299_300del
ENST00000527805.5:c.4084_4085del	ENSP00000435747.1:p.Ser1362HisfsTer2
ENST00000531525.2:c.91_92del	ENSP00000434327.2:p.Ser31HisfsTer2
ENST00000533733.5:n.513_514del
NM_000051.3:c.4084_4085del , LRG_135t1:c.4084_4085del	NP_000042.3:p.Ser1362HisfsTer2
XM_005271561.3:c.4084_4085del	XP_005271618.2:p.Ser1362HisfsTer2
XM_005271562.3:c.4084_4085del	XP_005271619.2:p.Ser1362HisfsTer2
XM_006718843.2:c.4084_4085del	XP_006718906.1:p.Ser1362HisfsTer2
XM_006718845.1:c.40_41del	XP_006718908.1:p.Ser14HisfsTer2
XM_011542840.1:c.4084_4085del	XP_011541142.1:p.Ser1362HisfsTer2
XM_011542841.1:c.4084_4085del	XP_011541143.1:p.Ser1362HisfsTer2
XM_011542842.1:c.3919_3920del	XP_011541144.1:p.Ser1307HisfsTer2
XM_011542843.1:c.4084_4085del	XP_011541145.1:p.Ser1362HisfsTer2
XM_011542844.1:c.3040_3041del	XP_011541146.1:p.Ser1014HisfsTer2
XM_011542845.1:c.2776_2777del	XP_011541147.1:p.Ser926HisfsTer2
XM_011542846.1:c.4084_4085del	XP_011541148.1:p.Ser1362HisfsTer2
NM_001351834.1:c.4084_4085del	NP_001338763.1:p.Ser1362HisfsTer2
XM_005271562.5:c.4084_4085del	XP_005271619.2:p.Ser1362HisfsTer2
XM_006718843.4:c.4084_4085del	XP_006718906.1:p.Ser1362HisfsTer2
XM_006718845.2:c.40_41del	XP_006718908.1:p.Ser14HisfsTer2
XM_011542840.3:c.4084_4085del	XP_011541142.1:p.Ser1362HisfsTer2
XM_011542842.3:c.3919_3920del	XP_011541144.1:p.Ser1307HisfsTer2
XM_011542843.2:c.4084_4085del	XP_011541145.1:p.Ser1362HisfsTer2
XM_011542844.3:c.3040_3041del	XP_011541146.1:p.Ser1014HisfsTer2
XM_011542845.2:c.2776_2777del	XP_011541147.1:p.Ser926HisfsTer2
XM_017017789.2:c.4084_4085del	XP_016873278.1:p.Ser1362HisfsTer2
XM_017017790.2:c.4084_4085del	XP_016873279.1:p.Ser1362HisfsTer2
XM_017017791.1:c.4084_4085del	XP_016873280.1:p.Ser1362HisfsTer2
XM_017017792.2:c.4084_4085del	XP_016873281.1:p.Ser1362HisfsTer2
XR_002957150.1:n.4817_4818del
NM_001351834.2:c.4084_4085del	NP_001338763.1:p.Ser1362HisfsTer2
NM_000051.4:c.4084_4085del MANE Select	NP_000042.3:p.Ser1362HisfsTer2