Canonical Allele Identifier: CA1998801294
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108304739C= , CM000673.2:g.108304739C= GRCh38
NC_000011.9:g.108175466C= , CM000673.1:g.108175466C= GRCh37
NC_000011.8:g.107680676C= NCBI36
NG_009830.1:g.86908C= , LRG_135:g.86908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.5561C= ENSP00000388058.2:p.Thr1854=
ENST00000713593.1:c.*5032C= ENSP00000518889.1:n.*5032C=
ENST00000278616.9:c.5561C= ENSP00000278616.4:p.Thr1854=
ENST00000683174.1:n.7045C=
ENST00000683524.1:n.785C=
ENST00000684152.1:n.1275C=
ENST00000527805.6:c.*625C= ENSP00000435747.2:n.*625C=
ENST00000675595.1:c.*625C= ENSP00000502563.1:n.*625C=
ENST00000675843.1:c.5561C= MANE Select ENSP00000501606.1:p.Thr1854=
ENST00000278616.8:c.5561C= ENSP00000278616.4:p.Thr1854=
ENST00000452508.6:c.5561C= ENSP00000388058.2:p.Thr1854=
ENST00000524792.5:n.1776C=
ENST00000529588.5:c.73C=
ENST00000533690.5:n.965C=
NM_000051.3:c.5561C= , LRG_135t1:c.5561C= NP_000042.3:p.Thr1854=
XM_005271561.3:c.5561C= XP_005271618.2:p.Thr1854=
XM_005271562.3:c.5561C= XP_005271619.2:p.Thr1854=
XM_006718843.2:c.5561C= XP_006718906.1:p.Thr1854=
XM_006718845.1:c.1517C= XP_006718908.1:p.Thr506=
XM_011542840.1:c.5561C= XP_011541142.1:p.Thr1854=
XM_011542841.1:c.5561C= XP_011541143.1:p.Thr1854=
XM_011542842.1:c.5396C= XP_011541144.1:p.Thr1799=
XM_011542843.1:c.5561C= XP_011541145.1:p.Thr1854=
XM_011542844.1:c.4517C= XP_011541146.1:p.Thr1506=
XM_011542845.1:c.4253C= XP_011541147.1:p.Thr1418=
XM_011542847.1:c.632C= XP_011541149.1:p.Thr211=
NM_001351834.1:c.5561C= NP_001338763.1:p.Thr1854=
XM_005271562.5:c.5561C= XP_005271619.2:p.Thr1854=
XM_006718843.4:c.5561C= XP_006718906.1:p.Thr1854=
XM_006718845.2:c.1517C= XP_006718908.1:p.Thr506=
XM_011542840.3:c.5561C= XP_011541142.1:p.Thr1854=
XM_011542842.3:c.5396C= XP_011541144.1:p.Thr1799=
XM_011542843.2:c.5561C= XP_011541145.1:p.Thr1854=
XM_011542844.3:c.4517C= XP_011541146.1:p.Thr1506=
XM_011542845.2:c.4253C= XP_011541147.1:p.Thr1418=
XM_017017789.2:c.5561C= XP_016873278.1:p.Thr1854=
XM_017017790.2:c.5561C= XP_016873279.1:p.Thr1854=
XM_017017791.1:c.5561C= XP_016873280.1:p.Thr1854=
XR_002957150.1:n.6161C=
NM_001351834.2:c.5561C= NP_001338763.1:p.Thr1854=
NM_000051.4:c.5561C= MANE Select NP_000042.3:p.Thr1854=