Canonical Allele Identifier: CA1998770812
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108250794A= , CM000673.2:g.108250794A= GRCh38
NC_000011.9:g.108121521A= , CM000673.1:g.108121521A= GRCh37
NC_000011.8:g.107626731A= NCBI36
NG_009830.1:g.32963A= , LRG_135:g.32963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.1329A= ENSP00000388058.2:p.Leu443=
ENST00000713593.1:c.*800A= ENSP00000518889.1:n.*800A=
ENST00000278616.9:c.1329A= ENSP00000278616.4:p.Leu443=
ENST00000682516.1:n.1463A=
ENST00000682956.1:n.1463A=
ENST00000683174.1:n.1479A=
ENST00000683605.1:n.824A=
ENST00000684037.1:c.*264A= ENSP00000508245.1:n.*264A=
ENST00000684061.1:n.1463A=
ENST00000684179.1:n.1298A=
ENST00000527805.6:c.1329A= ENSP00000435747.2:p.Leu443=
ENST00000675595.1:c.1164A= ENSP00000502563.1:p.Leu388=
ENST00000675843.1:c.1329A= MANE Select ENSP00000501606.1:p.Leu443=
ENST00000278616.8:c.1329A= ENSP00000278616.4:p.Leu443=
ENST00000452508.6:c.1329A= ENSP00000388058.2:p.Leu443=
ENST00000527805.5:c.1329A= ENSP00000435747.1:p.Leu443=
NM_000051.3:c.1329A= , LRG_135t1:c.1329A= NP_000042.3:p.Leu443=
XM_005271561.3:c.1329A= XP_005271618.2:p.Leu443=
XM_005271562.3:c.1329A= XP_005271619.2:p.Leu443=
XM_006718843.2:c.1329A= XP_006718906.1:p.Leu443=
XM_011542840.1:c.1329A= XP_011541142.1:p.Leu443=
XM_011542841.1:c.1329A= XP_011541143.1:p.Leu443=
XM_011542842.1:c.1164A= XP_011541144.1:p.Leu388=
XM_011542843.1:c.1329A= XP_011541145.1:p.Leu443=
XM_011542844.1:c.285A= XP_011541146.1:p.Leu95=
XM_011542845.1:c.21A= XP_011541147.1:p.Leu7=
XM_011542846.1:c.1329A= XP_011541148.1:p.Leu443=
NM_001351834.1:c.1329A= NP_001338763.1:p.Leu443=
XM_005271562.5:c.1329A= XP_005271619.2:p.Leu443=
XM_006718843.4:c.1329A= XP_006718906.1:p.Leu443=
XM_011542840.3:c.1329A= XP_011541142.1:p.Leu443=
XM_011542842.3:c.1164A= XP_011541144.1:p.Leu388=
XM_011542843.2:c.1329A= XP_011541145.1:p.Leu443=
XM_011542844.3:c.285A= XP_011541146.1:p.Leu95=
XM_011542845.2:c.21A= XP_011541147.1:p.Leu7=
XM_017017789.2:c.1329A= XP_016873278.1:p.Leu443=
XM_017017790.2:c.1329A= XP_016873279.1:p.Leu443=
XM_017017791.1:c.1329A= XP_016873280.1:p.Leu443=
XM_017017792.2:c.1329A= XP_016873281.1:p.Leu443=
XR_002957150.1:n.2062A=
NM_001351834.2:c.1329A= NP_001338763.1:p.Leu443=
NM_000051.4:c.1329A= MANE Select NP_000042.3:p.Leu443=