Canonical Allele Identifier: CA1998801239
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108304706C= , CM000673.2:g.108304706C= GRCh38
NC_000011.9:g.108175433C= , CM000673.1:g.108175433C= GRCh37
NC_000011.8:g.107680643C= NCBI36
NG_009830.1:g.86875C= , LRG_135:g.86875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.5528C= ENSP00000388058.2:p.Pro1843=
ENST00000713593.1:c.*4999C= ENSP00000518889.1:n.*4999C=
ENST00000278616.9:c.5528C= ENSP00000278616.4:p.Pro1843=
ENST00000683174.1:n.7012C=
ENST00000683524.1:n.752C=
ENST00000684152.1:n.1242C=
ENST00000527805.6:c.*592C= ENSP00000435747.2:n.*592C=
ENST00000675595.1:c.*592C= ENSP00000502563.1:n.*592C=
ENST00000675843.1:c.5528C= MANE Select ENSP00000501606.1:p.Pro1843=
ENST00000278616.8:c.5528C= ENSP00000278616.4:p.Pro1843=
ENST00000452508.6:c.5528C= ENSP00000388058.2:p.Pro1843=
ENST00000524792.5:n.1743C=
ENST00000529588.5:c.40C=
ENST00000533690.5:n.932C=
NM_000051.3:c.5528C= , LRG_135t1:c.5528C= NP_000042.3:p.Pro1843=
XM_005271561.3:c.5528C= XP_005271618.2:p.Pro1843=
XM_005271562.3:c.5528C= XP_005271619.2:p.Pro1843=
XM_006718843.2:c.5528C= XP_006718906.1:p.Pro1843=
XM_006718845.1:c.1484C= XP_006718908.1:p.Pro495=
XM_011542840.1:c.5528C= XP_011541142.1:p.Pro1843=
XM_011542841.1:c.5528C= XP_011541143.1:p.Pro1843=
XM_011542842.1:c.5363C= XP_011541144.1:p.Pro1788=
XM_011542843.1:c.5528C= XP_011541145.1:p.Pro1843=
XM_011542844.1:c.4484C= XP_011541146.1:p.Pro1495=
XM_011542845.1:c.4220C= XP_011541147.1:p.Pro1407=
XM_011542847.1:c.599C= XP_011541149.1:p.Pro200=
NM_001351834.1:c.5528C= NP_001338763.1:p.Pro1843=
XM_005271562.5:c.5528C= XP_005271619.2:p.Pro1843=
XM_006718843.4:c.5528C= XP_006718906.1:p.Pro1843=
XM_006718845.2:c.1484C= XP_006718908.1:p.Pro495=
XM_011542840.3:c.5528C= XP_011541142.1:p.Pro1843=
XM_011542842.3:c.5363C= XP_011541144.1:p.Pro1788=
XM_011542843.2:c.5528C= XP_011541145.1:p.Pro1843=
XM_011542844.3:c.4484C= XP_011541146.1:p.Pro1495=
XM_011542845.2:c.4220C= XP_011541147.1:p.Pro1407=
XM_017017789.2:c.5528C= XP_016873278.1:p.Pro1843=
XM_017017790.2:c.5528C= XP_016873279.1:p.Pro1843=
XM_017017791.1:c.5528C= XP_016873280.1:p.Pro1843=
XR_002957150.1:n.6128C=
NM_001351834.2:c.5528C= NP_001338763.1:p.Pro1843=
NM_000051.4:c.5528C= MANE Select NP_000042.3:p.Pro1843=