Canonical Allele Identifier: CA16041397
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 370563
ClinVar RCV Id: RCV000411095
dbSNP Id: rs1057516590

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108271397del , CM000673.2:g.108271397del GRCh38
NC_000011.9:g.108142124del , CM000673.1:g.108142124del GRCh37
NC_000011.8:g.107647334del NCBI36
NG_009830.1:g.53566del , LRG_135:g.53566del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.3068del ENSP00000388058.2:p.Gly1023GlufsTer6
ENST00000713593.1:c.*2539del ENSP00000518889.1:n.*2539del
ENST00000278616.9:c.3068del ENSP00000278616.4:p.Gly1023GlufsTer6
ENST00000682516.1:n.3002del
ENST00000683174.1:n.3218del
ENST00000684037.1:c.*1803del ENSP00000508245.1:n.*1803del
ENST00000527805.6:c.3068del ENSP00000435747.2:p.Gly1023GlufsTer6
ENST00000675595.1:c.2903del ENSP00000502563.1:p.Gly968GlufsTer6
ENST00000675843.1:c.3068del MANE Select ENSP00000501606.1:p.Gly1023GlufsTer6
ENST00000278616.8:c.3068del ENSP00000278616.4:p.Gly1023GlufsTer6
ENST00000452508.6:c.3068del ENSP00000388058.2:p.Gly1023GlufsTer6
ENST00000527805.5:c.3068del ENSP00000435747.1:p.Gly1023GlufsTer6
NM_000051.3:c.3068del , LRG_135t1:c.3068del NP_000042.3:p.Gly1023GlufsTer6
XM_005271561.3:c.3068del XP_005271618.2:p.Gly1023GlufsTer6
XM_005271562.3:c.3068del XP_005271619.2:p.Gly1023GlufsTer6
XM_006718843.2:c.3068del XP_006718906.1:p.Gly1023GlufsTer6
XM_011542840.1:c.3068del XP_011541142.1:p.Gly1023GlufsTer6
XM_011542841.1:c.3068del XP_011541143.1:p.Gly1023GlufsTer6
XM_011542842.1:c.2903del XP_011541144.1:p.Gly968GlufsTer6
XM_011542843.1:c.3068del XP_011541145.1:p.Gly1023GlufsTer6
XM_011542844.1:c.2024del XP_011541146.1:p.Gly675GlufsTer6
XM_011542845.1:c.1760del XP_011541147.1:p.Gly587GlufsTer6
XM_011542846.1:c.3068del XP_011541148.1:p.Gly1023GlufsTer6
NM_001351834.1:c.3068del NP_001338763.1:p.Gly1023GlufsTer6
XM_005271562.5:c.3068del XP_005271619.2:p.Gly1023GlufsTer6
XM_006718843.4:c.3068del XP_006718906.1:p.Gly1023GlufsTer6
XM_011542840.3:c.3068del XP_011541142.1:p.Gly1023GlufsTer6
XM_011542842.3:c.2903del XP_011541144.1:p.Gly968GlufsTer6
XM_011542843.2:c.3068del XP_011541145.1:p.Gly1023GlufsTer6
XM_011542844.3:c.2024del XP_011541146.1:p.Gly675GlufsTer6
XM_011542845.2:c.1760del XP_011541147.1:p.Gly587GlufsTer6
XM_017017789.2:c.3068del XP_016873278.1:p.Gly1023GlufsTer6
XM_017017790.2:c.3068del XP_016873279.1:p.Gly1023GlufsTer6
XM_017017791.1:c.3068del XP_016873280.1:p.Gly1023GlufsTer6
XM_017017792.2:c.3068del XP_016873281.1:p.Gly1023GlufsTer6
XR_002957150.1:n.3801del
NM_001351834.2:c.3068del NP_001338763.1:p.Gly1023GlufsTer6
NM_000051.4:c.3068del MANE Select NP_000042.3:p.Gly1023GlufsTer6