Canonical Allele Identifier: CA2615844904
Gene: ATM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108222983_108222984insC , CM000673.2:g.108222983_108222984insC GRCh38
NC_000011.9:g.108093710_108093711insC , CM000673.1:g.108093710_108093711insC GRCh37
NC_000011.8:g.107598920_107598921insC NCBI36
NG_009830.1:g.5152_5153insC , LRG_135:g.5152_5153insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-322_-321insC ENSP00000388058.2:n.-322_-321insC
ENST00000683914.2:c.-234_-233insC ENSP00000507649.1:n.-234_-233insC
ENST00000278616.8:c.-234_-233insC ENSP00000278616.4:n.-234_-233insC
ENST00000527805.5:c.-234_-233insC ENSP00000435747.1:n.-234_-233insC
NM_000051.3:c.-234_-233insC , LRG_135t1:c.-234_-233insC NP_000042.3:n.-234_-233insC
XM_011542843.1:c.-234_-233insC XP_011541145.1:n.-234_-233insC
XM_011542846.1:c.-234_-233insC XP_011541148.1:n.-234_-233insC
NM_001351834.1:c.-322_-321insC NP_001338763.1:n.-322_-321insC
NM_001351835.1:c.-234_-233insC NP_001338764.1:n.-234_-233insC
XM_011542842.3:c.-234_-233insC XP_011541144.1:n.-234_-233insC
XM_011542843.2:c.-234_-233insC XP_011541145.1:n.-234_-233insC
XM_011542844.3:c.-1256_-1255insC XP_011541146.1:n.-1256_-1255insC
XM_017017791.1:c.-234_-233insC XP_016873280.1:n.-234_-233insC
XM_017017792.2:c.-234_-233insC XP_016873281.1:n.-234_-233insC
XR_002957150.1:n.500_501insC