Canonical Allele Identifier: CA2615849527

Gene: ATM

Linked Data

• ClinVar Variation Id: 2891630
• ClinVar RCV Id: RCV003606727
• gnomAD v4: 11-108287682-CCAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108287686_108287689del , CM000673.2:g.108287686_108287689del	GRCh38
NC_000011.9:g.108158413_108158416del , CM000673.1:g.108158413_108158416del	GRCh37
NC_000011.8:g.107663623_107663626del	NCBI36
NG_009830.1:g.69855_69858del , LRG_135:g.69855_69858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4080_4083del	ENSP00000388058.2:p.Ser1360ArgfsTer25
ENST00000713593.1:c.*3551_*3554del	ENSP00000518889.1:n.*3551_*3554del
ENST00000278616.9:c.4080_4083del	ENSP00000278616.4:p.Ser1360ArgfsTer25
ENST00000533733.6:n.1343_1346del
ENST00000683174.1:n.4230_4233del
ENST00000527805.6:c.4080_4083del	ENSP00000435747.2:p.Ser1360ArgfsTer25
ENST00000675595.1:c.3915_3918del	ENSP00000502563.1:p.Ser1305ArgfsTer25
ENST00000675843.1:c.4080_4083del MANE Select	ENSP00000501606.1:p.Ser1360ArgfsTer25
ENST00000278616.8:c.4080_4083del	ENSP00000278616.4:p.Ser1360ArgfsTer25
ENST00000452508.6:c.4080_4083del	ENSP00000388058.2:p.Ser1360ArgfsTer25
ENST00000524792.5:n.295_298del
ENST00000527805.5:c.4080_4083del	ENSP00000435747.1:p.Ser1360ArgfsTer?
ENST00000531525.2:c.87_90del	ENSP00000434327.2:p.Ser29ArgfsTer25
ENST00000533733.5:n.509_512del
NM_000051.3:c.4080_4083del , LRG_135t1:c.4080_4083del	NP_000042.3:p.Ser1360ArgfsTer25
XM_005271561.3:c.4080_4083del	XP_005271618.2:p.Ser1360ArgfsTer25
XM_005271562.3:c.4080_4083del	XP_005271619.2:p.Ser1360ArgfsTer25
XM_006718843.2:c.4080_4083del	XP_006718906.1:p.Ser1360ArgfsTer25
XM_006718845.1:c.36_39del	XP_006718908.1:p.Ser12ArgfsTer25
XM_011542840.1:c.4080_4083del	XP_011541142.1:p.Ser1360ArgfsTer25
XM_011542841.1:c.4080_4083del	XP_011541143.1:p.Ser1360ArgfsTer25
XM_011542842.1:c.3915_3918del	XP_011541144.1:p.Ser1305ArgfsTer25
XM_011542843.1:c.4080_4083del	XP_011541145.1:p.Ser1360ArgfsTer25
XM_011542844.1:c.3036_3039del	XP_011541146.1:p.Ser1012ArgfsTer25
XM_011542845.1:c.2772_2775del	XP_011541147.1:p.Ser924ArgfsTer25
XM_011542846.1:c.4080_4083del	XP_011541148.1:p.Ser1360ArgfsTer25
NM_001351834.1:c.4080_4083del	NP_001338763.1:p.Ser1360ArgfsTer25
XM_005271562.5:c.4080_4083del	XP_005271619.2:p.Ser1360ArgfsTer25
XM_006718843.4:c.4080_4083del	XP_006718906.1:p.Ser1360ArgfsTer25
XM_006718845.2:c.36_39del	XP_006718908.1:p.Ser12ArgfsTer25
XM_011542840.3:c.4080_4083del	XP_011541142.1:p.Ser1360ArgfsTer25
XM_011542842.3:c.3915_3918del	XP_011541144.1:p.Ser1305ArgfsTer25
XM_011542843.2:c.4080_4083del	XP_011541145.1:p.Ser1360ArgfsTer25
XM_011542844.3:c.3036_3039del	XP_011541146.1:p.Ser1012ArgfsTer25
XM_011542845.2:c.2772_2775del	XP_011541147.1:p.Ser924ArgfsTer25
XM_017017789.2:c.4080_4083del	XP_016873278.1:p.Ser1360ArgfsTer25
XM_017017790.2:c.4080_4083del	XP_016873279.1:p.Ser1360ArgfsTer25
XM_017017791.1:c.4080_4083del	XP_016873280.1:p.Ser1360ArgfsTer25
XM_017017792.2:c.4080_4083del	XP_016873281.1:p.Ser1360ArgfsTer25
XR_002957150.1:n.4813_4816del
NM_001351834.2:c.4080_4083del	NP_001338763.1:p.Ser1360ArgfsTer25
NM_000051.4:c.4080_4083del MANE Select	NP_000042.3:p.Ser1360ArgfsTer25