Canonical Allele Identifier: CA916079969
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108284358_108287600dup , CM000673.2:g.108284358_108287600dup GRCh38
NC_000011.9:g.108155085_108158327dup , CM000673.1:g.108155085_108158327dup GRCh37
NC_000011.8:g.107660295_107663537dup NCBI36
NG_009830.1:g.66527_69769dup , LRG_135:g.66527_69769dup

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.3878_3994dup
ENST00000713593.1:c.*3349_*3465dup
ENST00000278616.9:c.3878_3994dup
ENST00000683174.1:n.4028_4144dup
ENST00000527805.6:c.3878_3994dup
ENST00000675595.1:c.3713_3829dup
ENST00000675843.1:c.3878_3994dup
ENST00000278616.8:c.3878_3994dup
ENST00000452508.6:c.3878_3994dup
ENST00000527805.5:c.3878_3994dup
NM_000051.3:c.3878_3994dup , LRG_135t1:c.3878_3994dup
XM_005271561.3:c.3878_3994dup
XM_005271562.3:c.3878_3994dup
XM_006718843.2:c.3878_3994dup
XM_011542840.1:c.3878_3994dup
XM_011542841.1:c.3878_3994dup
XM_011542842.1:c.3713_3829dup
XM_011542843.1:c.3878_3994dup
XM_011542844.1:c.2834_2950dup
XM_011542845.1:c.2570_2686dup
XM_011542846.1:c.3878_3994dup
NM_001351834.1:c.3878_3994dup
XM_005271562.5:c.3878_3994dup
XM_006718843.4:c.3878_3994dup
XM_011542840.3:c.3878_3994dup
XM_011542842.3:c.3713_3829dup
XM_011542843.2:c.3878_3994dup
XM_011542844.3:c.2834_2950dup
XM_011542845.2:c.2570_2686dup
XM_017017789.2:c.3878_3994dup
XM_017017790.2:c.3878_3994dup
XM_017017791.1:c.3878_3994dup
XM_017017792.2:c.3878_3994dup
XR_002957150.1:n.4611_4727dup
NM_001351834.2:c.3878_3994dup
NM_000051.4:c.3878_3994dup