Canonical Allele Identifier: CA1998758087
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108223126T= , CM000673.2:g.108223126T= GRCh38
NC_000011.9:g.108093853T= , CM000673.1:g.108093853T= GRCh37
NC_000011.8:g.107599063T= NCBI36
NG_009830.1:g.5295T= , LRG_135:g.5295T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-179T= ENSP00000388058.2:n.-179T=
ENST00000683914.2:c.-91T= ENSP00000507649.1:n.-91T=
ENST00000713593.1:c.-91T= ENSP00000518889.1:n.-91T=
ENST00000683174.1:n.60T=
ENST00000683468.1:c.-4499T= ENSP00000508178.1:n.-4499T=
ENST00000683488.1:n.83T=
ENST00000527805.6:c.-91T= ENSP00000435747.2:n.-91T=
ENST00000675595.1:c.-91T= ENSP00000502563.1:n.-91T=
ENST00000675843.1:c.-91T= MANE Select ENSP00000501606.1:n.-91T=
ENST00000278616.8:c.-91T= ENSP00000278616.4:n.-91T=
ENST00000452508.6:c.-179T= ENSP00000388058.2:n.-179T=
ENST00000527805.5:c.-91T= ENSP00000435747.1:n.-91T=
ENST00000527891.5:c.-91T= ENSP00000433955.1:n.-91T=
ENST00000530958.5:c.-4499T= ENSP00000483338.1:n.-4499T=
ENST00000532931.5:c.-165T= ENSP00000432318.1:n.-165T=
NM_000051.3:c.-91T= , LRG_135t1:c.-91T= NP_000042.3:n.-91T=
XM_005271561.3:c.-179T= XP_005271618.2:n.-179T=
XM_011542841.1:c.-882T= XP_011541143.1:n.-882T=
XM_011542842.1:c.-91T= XP_011541144.1:n.-91T=
XM_011542843.1:c.-91T= XP_011541145.1:n.-91T=
XM_011542846.1:c.-91T= XP_011541148.1:n.-91T=
NM_001351834.1:c.-179T= NP_001338763.1:n.-179T=
NM_001351835.1:c.-91T= NP_001338764.1:n.-91T=
XM_011542842.3:c.-91T= XP_011541144.1:n.-91T=
XM_011542843.2:c.-91T= XP_011541145.1:n.-91T=
XM_011542844.3:c.-1113T= XP_011541146.1:n.-1113T=
XM_017017791.1:c.-91T= XP_016873280.1:n.-91T=
XM_017017792.2:c.-91T= XP_016873281.1:n.-91T=
XR_002957150.1:n.643T=
NM_001351834.2:c.-179T= NP_001338763.1:n.-179T=
NM_000051.4:c.-91T= MANE Select NP_000042.3:n.-91T=
NM_001351835.2:c.-91T= NP_001338764.1:n.-91T=