Canonical Allele Identifier: CA382545537

Gene: ATM

Linked Data

• ClinVar Variation Id: 1054020
• ClinVar RCV Id: RCV001362458
• dbSNP Id: rs1591594506
• gnomAD v4: 11-108268546-G-T
• MyVariant Identifiers: chr11:g.108139273G>T (hg19) ; chr11:g.108268546G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108268546G>T , CM000673.2:g.108268546G>T	GRCh38
NC_000011.9:g.108139273G>T , CM000673.1:g.108139273G>T	GRCh37
NC_000011.8:g.107644483G>T	NCBI36
NG_009830.1:g.50715G>T , LRG_135:g.50715G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.2775G>T	ENSP00000388058.2:p.Arg925Ser
ENST00000713593.1:c.*2246G>T	ENSP00000518889.1:n.*2246G>T
ENST00000278616.9:c.2775G>T	ENSP00000278616.4:p.Arg925Ser
ENST00000682516.1:n.2772+1204G>T
ENST00000683174.1:n.2925G>T
ENST00000684037.1:c.*1573+1204G>T	ENSP00000508245.1:n.*1573+1204G>T
ENST00000527805.6:c.2775G>T	ENSP00000435747.2:p.Arg925Ser
ENST00000675595.1:c.2610G>T	ENSP00000502563.1:p.Arg870Ser
ENST00000675843.1:c.2775G>T MANE Select	ENSP00000501606.1:p.Arg925Ser
ENST00000278616.8:c.2775G>T	ENSP00000278616.4:p.Arg925Ser
ENST00000419286.2:n.137G>T
ENST00000452508.6:c.2775G>T	ENSP00000388058.2:p.Arg925Ser
ENST00000527805.5:c.2775G>T	ENSP00000435747.1:p.Arg925Ser
NM_000051.3:c.2775G>T , LRG_135t1:c.2775G>T	NP_000042.3:p.Arg925Ser
XM_005271561.3:c.2775G>T	XP_005271618.2:p.Arg925Ser
XM_005271562.3:c.2775G>T	XP_005271619.2:p.Arg925Ser
XM_006718843.2:c.2775G>T	XP_006718906.1:p.Arg925Ser
XM_011542840.1:c.2775G>T	XP_011541142.1:p.Arg925Ser
XM_011542841.1:c.2775G>T	XP_011541143.1:p.Arg925Ser
XM_011542842.1:c.2610G>T	XP_011541144.1:p.Arg870Ser
XM_011542843.1:c.2775G>T	XP_011541145.1:p.Arg925Ser
XM_011542844.1:c.1731G>T	XP_011541146.1:p.Arg577Ser
XM_011542845.1:c.1467G>T	XP_011541147.1:p.Arg489Ser
XM_011542846.1:c.2775G>T	XP_011541148.1:p.Arg925Ser
NM_001351834.1:c.2775G>T	NP_001338763.1:p.Arg925Ser
XM_005271562.5:c.2775G>T	XP_005271619.2:p.Arg925Ser
XM_006718843.4:c.2775G>T	XP_006718906.1:p.Arg925Ser
XM_011542840.3:c.2775G>T	XP_011541142.1:p.Arg925Ser
XM_011542842.3:c.2610G>T	XP_011541144.1:p.Arg870Ser
XM_011542843.2:c.2775G>T	XP_011541145.1:p.Arg925Ser
XM_011542844.3:c.1731G>T	XP_011541146.1:p.Arg577Ser
XM_011542845.2:c.1467G>T	XP_011541147.1:p.Arg489Ser
XM_017017789.2:c.2775G>T	XP_016873278.1:p.Arg925Ser
XM_017017790.2:c.2775G>T	XP_016873279.1:p.Arg925Ser
XM_017017791.1:c.2775G>T	XP_016873280.1:p.Arg925Ser
XM_017017792.2:c.2775G>T	XP_016873281.1:p.Arg925Ser
XR_002957150.1:n.3508G>T
NM_001351834.2:c.2775G>T	NP_001338763.1:p.Arg925Ser
NM_000051.4:c.2775G>T MANE Select	NP_000042.3:p.Arg925Ser