Canonical Allele Identifier: CA1998757814
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108222912A= , CM000673.2:g.108222912A= GRCh38
NC_000011.9:g.108093639A= , CM000673.1:g.108093639A= GRCh37
NC_000011.8:g.107598849A= NCBI36
NG_009830.1:g.5081A= , LRG_135:g.5081A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-393A= ENSP00000388058.2:n.-393A=
ENST00000683914.2:c.-305A= ENSP00000507649.1:n.-305A=
ENST00000278616.8:c.-305A= ENSP00000278616.4:n.-305A=
ENST00000527805.5:c.-305A= ENSP00000435747.1:n.-305A=
NM_000051.3:c.-305A= , LRG_135t1:c.-305A= NP_000042.3:n.-305A=
XM_011542843.1:c.-305A= XP_011541145.1:n.-305A=
XM_011542846.1:c.-305A= XP_011541148.1:n.-305A=
NM_001351834.1:c.-393A= NP_001338763.1:n.-393A=
NM_001351835.1:c.-305A= NP_001338764.1:n.-305A=
XM_011542842.3:c.-305A= XP_011541144.1:n.-305A=
XM_011542843.2:c.-305A= XP_011541145.1:n.-305A=
XM_011542844.3:c.-1327A= XP_011541146.1:n.-1327A=
XM_017017791.1:c.-305A= XP_016873280.1:n.-305A=
XM_017017792.2:c.-305A= XP_016873281.1:n.-305A=
XR_002957150.1:n.429A=