Canonical Allele Identifier: CA1998758102
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108223138C= , CM000673.2:g.108223138C= GRCh38
NC_000011.9:g.108093865C= , CM000673.1:g.108093865C= GRCh37
NC_000011.8:g.107599075C= NCBI36
NG_009830.1:g.5307C= , LRG_135:g.5307C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-167C= ENSP00000388058.2:n.-167C=
ENST00000683914.2:c.-79C= ENSP00000507649.1:n.-79C=
ENST00000713593.1:c.-79C= ENSP00000518889.1:n.-79C=
ENST00000683174.1:n.72C=
ENST00000683468.1:c.-4487C= ENSP00000508178.1:n.-4487C=
ENST00000683488.1:n.95C=
ENST00000527805.6:c.-79C= ENSP00000435747.2:n.-79C=
ENST00000675595.1:c.-79C= ENSP00000502563.1:n.-79C=
ENST00000675843.1:c.-79C= MANE Select ENSP00000501606.1:n.-79C=
ENST00000278616.8:c.-79C= ENSP00000278616.4:n.-79C=
ENST00000452508.6:c.-167C= ENSP00000388058.2:n.-167C=
ENST00000527805.5:c.-79C= ENSP00000435747.1:n.-79C=
ENST00000527891.5:c.-79C= ENSP00000433955.1:n.-79C=
ENST00000530958.5:c.-4487C= ENSP00000483338.1:n.-4487C=
ENST00000532931.5:c.-153C= ENSP00000432318.1:n.-153C=
NM_000051.3:c.-79C= , LRG_135t1:c.-79C= NP_000042.3:n.-79C=
XM_005271561.3:c.-167C= XP_005271618.2:n.-167C=
XM_011542841.1:c.-870C= XP_011541143.1:n.-870C=
XM_011542842.1:c.-79C= XP_011541144.1:n.-79C=
XM_011542843.1:c.-79C= XP_011541145.1:n.-79C=
XM_011542846.1:c.-79C= XP_011541148.1:n.-79C=
NM_001351834.1:c.-167C= NP_001338763.1:n.-167C=
NM_001351835.1:c.-79C= NP_001338764.1:n.-79C=
XM_011542842.3:c.-79C= XP_011541144.1:n.-79C=
XM_011542843.2:c.-79C= XP_011541145.1:n.-79C=
XM_011542844.3:c.-1101C= XP_011541146.1:n.-1101C=
XM_017017791.1:c.-79C= XP_016873280.1:n.-79C=
XM_017017792.2:c.-79C= XP_016873281.1:n.-79C=
XR_002957150.1:n.655C=
NM_001351834.2:c.-167C= NP_001338763.1:n.-167C=
NM_000051.4:c.-79C= MANE Select NP_000042.3:n.-79C=
NM_001351835.2:c.-79C= NP_001338764.1:n.-79C=