Canonical Allele Identifier: CA476744757

Gene: ATM

Linked Data

• ClinVar Variation Id: 928491
• ClinVar RCV Id: RCV001192415 ; RCV002559212 ; RCV003293978
• dbSNP Id: rs1290222131
• gnomAD v4: 11-108244920-T-A
• MyVariant Identifiers: chr11:g.108115647T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108244920T>A , CM000673.2:g.108244920T>A	GRCh38
NC_000011.9:g.108115647T>A , CM000673.1:g.108115647T>A	GRCh37
NC_000011.8:g.107620857T>A	NCBI36
NG_009830.1:g.27089T>A , LRG_135:g.27089T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.795T>A	ENSP00000388058.2:p.Ile265=
ENST00000713593.1:c.*266T>A	ENSP00000518889.1:n.*266T>A
ENST00000278616.9:c.795T>A	ENSP00000278616.4:p.Ile265=
ENST00000682430.1:n.894T>A
ENST00000682516.1:n.929T>A
ENST00000682956.1:n.929T>A
ENST00000683100.1:n.3142T>A
ENST00000683174.1:n.945T>A
ENST00000683605.1:n.290T>A
ENST00000684037.1:c.795T>A	ENSP00000508245.1:p.Ile265=
ENST00000684061.1:n.929T>A
ENST00000684179.1:n.764T>A
ENST00000527805.6:c.795T>A	ENSP00000435747.2:p.Ile265=
ENST00000675595.1:c.630T>A	ENSP00000502563.1:p.Ile210=
ENST00000675843.1:c.795T>A MANE Select	ENSP00000501606.1:p.Ile265=
ENST00000278616.8:c.795T>A	ENSP00000278616.4:p.Ile265=
ENST00000452508.6:c.795T>A	ENSP00000388058.2:p.Ile265=
ENST00000527805.5:c.795T>A	ENSP00000435747.1:p.Ile265=
NM_000051.3:c.795T>A , LRG_135t1:c.795T>A	NP_000042.3:p.Ile265=
XM_005271561.3:c.795T>A	XP_005271618.2:p.Ile265=
XM_005271562.3:c.795T>A	XP_005271619.2:p.Ile265=
XM_006718843.2:c.795T>A	XP_006718906.1:p.Ile265=
XM_011542840.1:c.795T>A	XP_011541142.1:p.Ile265=
XM_011542841.1:c.795T>A	XP_011541143.1:p.Ile265=
XM_011542842.1:c.630T>A	XP_011541144.1:p.Ile210=
XM_011542843.1:c.795T>A	XP_011541145.1:p.Ile265=
XM_011542844.1:c.-250T>A	XP_011541146.1:n.-250T>A
XM_011542846.1:c.795T>A	XP_011541148.1:p.Ile265=
NM_001351834.1:c.795T>A	NP_001338763.1:p.Ile265=
XM_005271562.5:c.795T>A	XP_005271619.2:p.Ile265=
XM_006718843.4:c.795T>A	XP_006718906.1:p.Ile265=
XM_011542840.3:c.795T>A	XP_011541142.1:p.Ile265=
XM_011542842.3:c.630T>A	XP_011541144.1:p.Ile210=
XM_011542843.2:c.795T>A	XP_011541145.1:p.Ile265=
XM_011542844.3:c.-250T>A	XP_011541146.1:n.-250T>A
XM_017017789.2:c.795T>A	XP_016873278.1:p.Ile265=
XM_017017790.2:c.795T>A	XP_016873279.1:p.Ile265=
XM_017017791.1:c.795T>A	XP_016873280.1:p.Ile265=
XM_017017792.2:c.795T>A	XP_016873281.1:p.Ile265=
XR_002957150.1:n.1528T>A
NM_001351834.2:c.795T>A	NP_001338763.1:p.Ile265=
NM_000051.4:c.795T>A MANE Select	NP_000042.3:p.Ile265=