Canonical Allele Identifier: CA1998757904
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs2078560922

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108222977C>T , CM000673.2:g.108222977C>T GRCh38
NC_000011.9:g.108093704C>T , CM000673.1:g.108093704C>T GRCh37
NC_000011.8:g.107598914C>T NCBI36
NG_009830.1:g.5146C>T , LRG_135:g.5146C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-328C>T ENSP00000388058.2:n.-328C>T
ENST00000683914.2:c.-240C>T ENSP00000507649.1:n.-240C>T
ENST00000278616.8:c.-240C>T ENSP00000278616.4:n.-240C>T
ENST00000527805.5:c.-240C>T ENSP00000435747.1:n.-240C>T
NM_000051.3:c.-240C>T , LRG_135t1:c.-240C>T NP_000042.3:n.-240C>T
XM_011542843.1:c.-240C>T XP_011541145.1:n.-240C>T
XM_011542846.1:c.-240C>T XP_011541148.1:n.-240C>T
NM_001351834.1:c.-328C>T NP_001338763.1:n.-328C>T
NM_001351835.1:c.-240C>T NP_001338764.1:n.-240C>T
XM_011542842.3:c.-240C>T XP_011541144.1:n.-240C>T
XM_011542843.2:c.-240C>T XP_011541145.1:n.-240C>T
XM_011542844.3:c.-1262C>T XP_011541146.1:n.-1262C>T
XM_017017791.1:c.-240C>T XP_016873280.1:n.-240C>T
XM_017017792.2:c.-240C>T XP_016873281.1:n.-240C>T
XR_002957150.1:n.494C>T