Canonical Allele Identifier: CA658656248
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453492
ClinVar RCV Id: RCV003470668
dbSNP Id: rs1555093289

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108284236_108284237dup , CM000673.2:g.108284236_108284237dup GRCh38
NC_000011.9:g.108154963_108154964dup , CM000673.1:g.108154963_108154964dup GRCh37
NC_000011.8:g.107660173_107660174dup NCBI36
NG_009830.1:g.66405_66406dup , LRG_135:g.66405_66406dup

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.3756_3757dup ENSP00000388058.2:p.Lys1253IlefsTer4
ENST00000713593.1:c.*3227_*3228dup ENSP00000518889.1:n.*3227_*3228dup
ENST00000278616.9:c.3756_3757dup ENSP00000278616.4:p.Lys1253IlefsTer4
ENST00000682289.1:n.103_104dup
ENST00000683174.1:n.3906_3907dup
ENST00000527805.6:c.3756_3757dup ENSP00000435747.2:p.Lys1253IlefsTer4
ENST00000675595.1:c.3591_3592dup ENSP00000502563.1:p.Lys1198IlefsTer4
ENST00000675843.1:c.3756_3757dup MANE Select ENSP00000501606.1:p.Lys1253IlefsTer4
ENST00000278616.8:c.3756_3757dup ENSP00000278616.4:p.Lys1253IlefsTer4
ENST00000452508.6:c.3756_3757dup ENSP00000388058.2:p.Lys1253IlefsTer4
ENST00000527805.5:c.3756_3757dup ENSP00000435747.1:p.Lys1253IlefsTer4
NM_000051.3:c.3756_3757dup , LRG_135t1:c.3756_3757dup NP_000042.3:p.Lys1253IlefsTer4
XM_005271561.3:c.3756_3757dup XP_005271618.2:p.Lys1253IlefsTer4
XM_005271562.3:c.3756_3757dup XP_005271619.2:p.Lys1253IlefsTer4
XM_006718843.2:c.3756_3757dup XP_006718906.1:p.Lys1253IlefsTer4
XM_011542840.1:c.3756_3757dup XP_011541142.1:p.Lys1253IlefsTer4
XM_011542841.1:c.3756_3757dup XP_011541143.1:p.Lys1253IlefsTer4
XM_011542842.1:c.3591_3592dup XP_011541144.1:p.Lys1198IlefsTer4
XM_011542843.1:c.3756_3757dup XP_011541145.1:p.Lys1253IlefsTer4
XM_011542844.1:c.2712_2713dup XP_011541146.1:p.Lys905IlefsTer4
XM_011542845.1:c.2448_2449dup XP_011541147.1:p.Lys817IlefsTer4
XM_011542846.1:c.3756_3757dup XP_011541148.1:p.Lys1253IlefsTer4
NM_001351834.1:c.3756_3757dup NP_001338763.1:p.Lys1253IlefsTer4
XM_005271562.5:c.3756_3757dup XP_005271619.2:p.Lys1253IlefsTer4
XM_006718843.4:c.3756_3757dup XP_006718906.1:p.Lys1253IlefsTer4
XM_011542840.3:c.3756_3757dup XP_011541142.1:p.Lys1253IlefsTer4
XM_011542842.3:c.3591_3592dup XP_011541144.1:p.Lys1198IlefsTer4
XM_011542843.2:c.3756_3757dup XP_011541145.1:p.Lys1253IlefsTer4
XM_011542844.3:c.2712_2713dup XP_011541146.1:p.Lys905IlefsTer4
XM_011542845.2:c.2448_2449dup XP_011541147.1:p.Lys817IlefsTer4
XM_017017789.2:c.3756_3757dup XP_016873278.1:p.Lys1253IlefsTer4
XM_017017790.2:c.3756_3757dup XP_016873279.1:p.Lys1253IlefsTer4
XM_017017791.1:c.3756_3757dup XP_016873280.1:p.Lys1253IlefsTer4
XM_017017792.2:c.3756_3757dup XP_016873281.1:p.Lys1253IlefsTer4
XR_002957150.1:n.4489_4490dup
NM_001351834.2:c.3756_3757dup NP_001338763.1:p.Lys1253IlefsTer4
NM_000051.4:c.3756_3757dup MANE Select NP_000042.3:p.Lys1253IlefsTer4