Canonical Allele Identifier: CA194117

Gene: ATM

Linked Data

• ClinVar Variation Id: 186194
• ClinVar RCV Id: RCV000165740 ; RCV000205331 ; RCV003330525 ; RCV003316048 ; RCV001706083
• dbSNP Id: rs786202765
• gnomAD v2: 11-108170580-G-A
• gnomAD v4: 11-108299853-G-A
• MyVariant Identifiers: chr11:g.108170580G>A (hg19) ; chr11:g.108299853G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108299853G>A , CM000673.2:g.108299853G>A	GRCh38
NC_000011.9:g.108170580G>A , CM000673.1:g.108170580G>A	GRCh37
NC_000011.8:g.107675790G>A	NCBI36
NG_009830.1:g.82022G>A , LRG_135:g.82022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5145G>A	ENSP00000388058.2:p.Leu1715=
ENST00000713593.1:c.*4616G>A	ENSP00000518889.1:n.*4616G>A
ENST00000278616.9:c.5145G>A	ENSP00000278616.4:p.Leu1715=
ENST00000683174.1:n.6629G>A
ENST00000683524.1:n.369G>A
ENST00000684152.1:n.859G>A
ENST00000527805.6:c.*209G>A	ENSP00000435747.2:n.*209G>A
ENST00000675595.1:c.*209G>A	ENSP00000502563.1:n.*209G>A
ENST00000675843.1:c.5145G>A MANE Select	ENSP00000501606.1:p.Leu1715=
ENST00000278616.8:c.5145G>A	ENSP00000278616.4:p.Leu1715=
ENST00000452508.6:c.5145G>A	ENSP00000388058.2:p.Leu1715=
ENST00000524792.5:n.1360G>A
ENST00000533690.5:n.549G>A
ENST00000534625.1:n.374G>A
NM_000051.3:c.5145G>A , LRG_135t1:c.5145G>A	NP_000042.3:p.Leu1715=
XM_005271561.3:c.5145G>A	XP_005271618.2:p.Leu1715=
XM_005271562.3:c.5145G>A	XP_005271619.2:p.Leu1715=
XM_006718843.2:c.5145G>A	XP_006718906.1:p.Leu1715=
XM_006718845.1:c.1101G>A	XP_006718908.1:p.Leu367=
XM_011542840.1:c.5145G>A	XP_011541142.1:p.Leu1715=
XM_011542841.1:c.5145G>A	XP_011541143.1:p.Leu1715=
XM_011542842.1:c.4980G>A	XP_011541144.1:p.Leu1660=
XM_011542843.1:c.5145G>A	XP_011541145.1:p.Leu1715=
XM_011542844.1:c.4101G>A	XP_011541146.1:p.Leu1367=
XM_011542845.1:c.3837G>A	XP_011541147.1:p.Leu1279=
XM_011542846.1:c.5145G>A	XP_011541148.1:p.Leu1715=
XM_011542847.1:c.216G>A	XP_011541149.1:p.Leu72=
NM_001351834.1:c.5145G>A	NP_001338763.1:p.Leu1715=
XM_005271562.5:c.5145G>A	XP_005271619.2:p.Leu1715=
XM_006718843.4:c.5145G>A	XP_006718906.1:p.Leu1715=
XM_006718845.2:c.1101G>A	XP_006718908.1:p.Leu367=
XM_011542840.3:c.5145G>A	XP_011541142.1:p.Leu1715=
XM_011542842.3:c.4980G>A	XP_011541144.1:p.Leu1660=
XM_011542843.2:c.5145G>A	XP_011541145.1:p.Leu1715=
XM_011542844.3:c.4101G>A	XP_011541146.1:p.Leu1367=
XM_011542845.2:c.3837G>A	XP_011541147.1:p.Leu1279=
XM_017017789.2:c.5145G>A	XP_016873278.1:p.Leu1715=
XM_017017790.2:c.5145G>A	XP_016873279.1:p.Leu1715=
XM_017017791.1:c.5145G>A	XP_016873280.1:p.Leu1715=
XM_017017792.2:c.5145G>A	XP_016873281.1:p.Leu1715=
XR_002957150.1:n.5745G>A
NM_001351834.2:c.5145G>A	NP_001338763.1:p.Leu1715=
NM_000051.4:c.5145G>A MANE Select	NP_000042.3:p.Leu1715=