Canonical Allele Identifier: CA382543040

Gene: ATM

Linked Data

• ClinVar Variation Id: 482731
• ClinVar RCV Id: RCV000564720 ; RCV000657611 ; RCV001218574 ; RCV004024502 ; RCV002497210
• dbSNP Id: rs1555106321
• MyVariant Identifiers: chr11:g.108173586G>T (hg19) ; chr11:g.108302859G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108302859G>T , CM000673.2:g.108302859G>T	GRCh38
NC_000011.9:g.108173586G>T , CM000673.1:g.108173586G>T	GRCh37
NC_000011.8:g.107678796G>T	NCBI36
NG_009830.1:g.85028G>T , LRG_135:g.85028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5326G>T	ENSP00000388058.2:p.Glu1776Ter
ENST00000713593.1:c.*4797G>T	ENSP00000518889.1:n.*4797G>T
ENST00000278616.9:c.5326G>T	ENSP00000278616.4:p.Glu1776Ter
ENST00000683174.1:n.6810G>T
ENST00000683524.1:n.550G>T
ENST00000684152.1:n.1040G>T
ENST00000527805.6:c.*390G>T	ENSP00000435747.2:n.*390G>T
ENST00000675595.1:c.*390G>T	ENSP00000502563.1:n.*390G>T
ENST00000675843.1:c.5326G>T MANE Select	ENSP00000501606.1:p.Glu1776Ter
ENST00000278616.8:c.5326G>T	ENSP00000278616.4:p.Glu1776Ter
ENST00000452508.6:c.5326G>T	ENSP00000388058.2:p.Glu1776Ter
ENST00000524792.5:n.1541G>T
ENST00000533690.5:n.730G>T
ENST00000534625.1:n.555G>T
NM_000051.3:c.5326G>T , LRG_135t1:c.5326G>T	NP_000042.3:p.Glu1776Ter
XM_005271561.3:c.5326G>T	XP_005271618.2:p.Glu1776Ter
XM_005271562.3:c.5326G>T	XP_005271619.2:p.Glu1776Ter
XM_006718843.2:c.5326G>T	XP_006718906.1:p.Glu1776Ter
XM_006718845.1:c.1282G>T	XP_006718908.1:p.Glu428Ter
XM_011542840.1:c.5326G>T	XP_011541142.1:p.Glu1776Ter
XM_011542841.1:c.5326G>T	XP_011541143.1:p.Glu1776Ter
XM_011542842.1:c.5161G>T	XP_011541144.1:p.Glu1721Ter
XM_011542843.1:c.5326G>T	XP_011541145.1:p.Glu1776Ter
XM_011542844.1:c.4282G>T	XP_011541146.1:p.Glu1428Ter
XM_011542845.1:c.4018G>T	XP_011541147.1:p.Glu1340Ter
XM_011542846.1:c.5327G>T	XP_011541148.1:p.Arg1776Ile
XM_011542847.1:c.397G>T	XP_011541149.1:p.Glu133Ter
NM_001351834.1:c.5326G>T	NP_001338763.1:p.Glu1776Ter
XM_005271562.5:c.5326G>T	XP_005271619.2:p.Glu1776Ter
XM_006718843.4:c.5326G>T	XP_006718906.1:p.Glu1776Ter
XM_006718845.2:c.1282G>T	XP_006718908.1:p.Glu428Ter
XM_011542840.3:c.5326G>T	XP_011541142.1:p.Glu1776Ter
XM_011542842.3:c.5161G>T	XP_011541144.1:p.Glu1721Ter
XM_011542843.2:c.5326G>T	XP_011541145.1:p.Glu1776Ter
XM_011542844.3:c.4282G>T	XP_011541146.1:p.Glu1428Ter
XM_011542845.2:c.4018G>T	XP_011541147.1:p.Glu1340Ter
XM_017017789.2:c.5326G>T	XP_016873278.1:p.Glu1776Ter
XM_017017790.2:c.5326G>T	XP_016873279.1:p.Glu1776Ter
XM_017017791.1:c.5326G>T	XP_016873280.1:p.Glu1776Ter
XM_017017792.2:c.*7G>T	XP_016873281.1:n.*7G>T
XR_002957150.1:n.5926G>T
NM_001351834.2:c.5326G>T	NP_001338763.1:p.Glu1776Ter
NM_000051.4:c.5326G>T MANE Select	NP_000042.3:p.Glu1776Ter