Canonical Allele Identifier: CA382544186

Gene: ATM

Linked Data

• ClinVar Variation Id: 453579
• ClinVar RCV Id: RCV000557051
• dbSNP Id: rs1555106518
• MyVariant Identifiers: chr11:g.108173705C>G (hg19) ; chr11:g.108302978C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108302978C>G , CM000673.2:g.108302978C>G	GRCh38
NC_000011.9:g.108173705C>G , CM000673.1:g.108173705C>G	GRCh37
NC_000011.8:g.107678915C>G	NCBI36
NG_009830.1:g.85147C>G , LRG_135:g.85147C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.5445C>G	ENSP00000388058.2:p.Asp1815Glu
ENST00000713593.1:c.*4916C>G	ENSP00000518889.1:n.*4916C>G
ENST00000278616.9:c.5445C>G	ENSP00000278616.4:p.Asp1815Glu
ENST00000683174.1:n.6929C>G
ENST00000683524.1:n.669C>G
ENST00000684152.1:n.1159C>G
ENST00000527805.6:c.*509C>G	ENSP00000435747.2:n.*509C>G
ENST00000675595.1:c.*509C>G	ENSP00000502563.1:n.*509C>G
ENST00000675843.1:c.5445C>G MANE Select	ENSP00000501606.1:p.Asp1815Glu
ENST00000278616.8:c.5445C>G	ENSP00000278616.4:p.Asp1815Glu
ENST00000452508.6:c.5445C>G	ENSP00000388058.2:p.Asp1815Glu
ENST00000524792.5:n.1660C>G
ENST00000533690.5:n.849C>G
ENST00000534625.1:n.674C>G
NM_000051.3:c.5445C>G , LRG_135t1:c.5445C>G	NP_000042.3:p.Asp1815Glu
XM_005271561.3:c.5445C>G	XP_005271618.2:p.Asp1815Glu
XM_005271562.3:c.5445C>G	XP_005271619.2:p.Asp1815Glu
XM_006718843.2:c.5445C>G	XP_006718906.1:p.Asp1815Glu
XM_006718845.1:c.1401C>G	XP_006718908.1:p.Asp467Glu
XM_011542840.1:c.5445C>G	XP_011541142.1:p.Asp1815Glu
XM_011542841.1:c.5445C>G	XP_011541143.1:p.Asp1815Glu
XM_011542842.1:c.5280C>G	XP_011541144.1:p.Asp1760Glu
XM_011542843.1:c.5445C>G	XP_011541145.1:p.Asp1815Glu
XM_011542844.1:c.4401C>G	XP_011541146.1:p.Asp1467Glu
XM_011542845.1:c.4137C>G	XP_011541147.1:p.Asp1379Glu
XM_011542847.1:c.516C>G	XP_011541149.1:p.Asp172Glu
NM_001351834.1:c.5445C>G	NP_001338763.1:p.Asp1815Glu
XM_005271562.5:c.5445C>G	XP_005271619.2:p.Asp1815Glu
XM_006718843.4:c.5445C>G	XP_006718906.1:p.Asp1815Glu
XM_006718845.2:c.1401C>G	XP_006718908.1:p.Asp467Glu
XM_011542840.3:c.5445C>G	XP_011541142.1:p.Asp1815Glu
XM_011542842.3:c.5280C>G	XP_011541144.1:p.Asp1760Glu
XM_011542843.2:c.5445C>G	XP_011541145.1:p.Asp1815Glu
XM_011542844.3:c.4401C>G	XP_011541146.1:p.Asp1467Glu
XM_011542845.2:c.4137C>G	XP_011541147.1:p.Asp1379Glu
XM_017017789.2:c.5445C>G	XP_016873278.1:p.Asp1815Glu
XM_017017790.2:c.5445C>G	XP_016873279.1:p.Asp1815Glu
XM_017017791.1:c.5445C>G	XP_016873280.1:p.Asp1815Glu
XR_002957150.1:n.6045C>G
NM_001351834.2:c.5445C>G	NP_001338763.1:p.Asp1815Glu
NM_000051.4:c.5445C>G MANE Select	NP_000042.3:p.Asp1815Glu