Canonical Allele Identifier: CA348209

Gene: ATM

Linked Data

• ClinVar Variation Id: 220555
• ClinVar RCV Id: RCV000203930 ; RCV000235749 ; RCV000563715
• dbSNP Id: rs772926890
• ExAC: 11:108121800 G / T
• gnomAD v2: 11-108121800-G-T
• gnomAD v4: 11-108251073-G-T
• MyVariant Identifiers: chr11:g.108121800G>T (hg19) ; chr11:g.108251073G>T (hg38)
• ERepo: CA348209/MONDO:0016419/020
• PubMed: PMID:9443866 ; PMID:9450906 ; PMID:10330348 ; PMID:17124347 ; PMID:19691550

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108251073G>T , CM000673.2:g.108251073G>T	GRCh38
NC_000011.9:g.108121800G>T , CM000673.1:g.108121800G>T	GRCh37
NC_000011.8:g.107627010G>T	NCBI36
NG_009830.1:g.33242G>T , LRG_135:g.33242G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.1607+1G>T	ENSP00000388058.2:n.1607+1G>T
ENST00000713593.1:c.*1078+1G>T	ENSP00000518889.1:n.*1078+1G>T
ENST00000278616.9:c.1607+1G>T	ENSP00000278616.4:n.1607+1G>T
ENST00000682516.1:n.1741+1G>T
ENST00000682956.1:n.1742G>T
ENST00000683174.1:n.1757+1G>T
ENST00000683605.1:n.1102+1G>T
ENST00000684037.1:c.*542+1G>T	ENSP00000508245.1:n.*542+1G>T
ENST00000684061.1:n.1741+1G>T
ENST00000684179.1:n.1577G>T
ENST00000527805.6:c.1607+1G>T	ENSP00000435747.2:n.1607+1G>T
ENST00000675595.1:c.1442+1G>T	ENSP00000502563.1:n.1442+1G>T
ENST00000675843.1:c.1607+1G>T MANE Select	ENSP00000501606.1:n.1607+1G>T
ENST00000278616.8:c.1607+1G>T	ENSP00000278616.4:n.1607+1G>T
ENST00000452508.6:c.1607+1G>T	ENSP00000388058.2:n.1607+1G>T
ENST00000527805.5:c.1607+1G>T	ENSP00000435747.1:n.1607+1G>T
NM_000051.3:c.1607+1G>T , LRG_135t1:c.1607+1G>T	NP_000042.3:n.1607+1G>T
XM_005271561.3:c.1607+1G>T	XP_005271618.2:n.1607+1G>T
XM_005271562.3:c.1607+1G>T	XP_005271619.2:n.1607+1G>T
XM_006718843.2:c.1607+1G>T	XP_006718906.1:n.1607+1G>T
XM_011542840.1:c.1607+1G>T	XP_011541142.1:n.1607+1G>T
XM_011542841.1:c.1607+1G>T	XP_011541143.1:n.1607+1G>T
XM_011542842.1:c.1442+1G>T	XP_011541144.1:n.1442+1G>T
XM_011542843.1:c.1607+1G>T	XP_011541145.1:n.1607+1G>T
XM_011542844.1:c.563+1G>T	XP_011541146.1:n.563+1G>T
XM_011542845.1:c.299+1G>T	XP_011541147.1:n.299+1G>T
XM_011542846.1:c.1607+1G>T	XP_011541148.1:n.1607+1G>T
NM_001351834.1:c.1607+1G>T	NP_001338763.1:n.1607+1G>T
XM_005271562.5:c.1607+1G>T	XP_005271619.2:n.1607+1G>T
XM_006718843.4:c.1607+1G>T	XP_006718906.1:n.1607+1G>T
XM_011542840.3:c.1607+1G>T	XP_011541142.1:n.1607+1G>T
XM_011542842.3:c.1442+1G>T	XP_011541144.1:n.1442+1G>T
XM_011542843.2:c.1607+1G>T	XP_011541145.1:n.1607+1G>T
XM_011542844.3:c.563+1G>T	XP_011541146.1:n.563+1G>T
XM_011542845.2:c.299+1G>T	XP_011541147.1:n.299+1G>T
XM_017017789.2:c.1607+1G>T	XP_016873278.1:n.1607+1G>T
XM_017017790.2:c.1607+1G>T	XP_016873279.1:n.1607+1G>T
XM_017017791.1:c.1607+1G>T	XP_016873280.1:n.1607+1G>T
XM_017017792.2:c.1607+1G>T	XP_016873281.1:n.1607+1G>T
XR_002957150.1:n.2340+1G>T
NM_001351834.2:c.1607+1G>T	NP_001338763.1:n.1607+1G>T
NM_000051.4:c.1607+1G>T MANE Select	NP_000042.3:n.1607+1G>T