Canonical Allele Identifier: CA192470

Gene: ATM

Linked Data

• ClinVar Variation Id: 185632
• ClinVar RCV Id: RCV000165081 ; RCV001704200 ; RCV001248472
• dbSNP Id: rs763473729
• ExAC: 11:108151766 T / C
• MyVariant Identifiers: chr11:g.108151766T>C (hg19) ; chr11:g.108281039T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108281039T>C , CM000673.2:g.108281039T>C	GRCh38
NC_000011.9:g.108151766T>C , CM000673.1:g.108151766T>C	GRCh37
NC_000011.8:g.107656976T>C	NCBI36
NG_009830.1:g.63208T>C , LRG_135:g.63208T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.3447T>C	ENSP00000388058.2:p.Asn1149=
ENST00000713593.1:c.*2918T>C	ENSP00000518889.1:n.*2918T>C
ENST00000278616.9:c.3447T>C	ENSP00000278616.4:p.Asn1149=
ENST00000683174.1:n.3597T>C
ENST00000527805.6:c.3447T>C	ENSP00000435747.2:p.Asn1149=
ENST00000675595.1:c.3282T>C	ENSP00000502563.1:p.Asn1094=
ENST00000675843.1:c.3447T>C MANE Select	ENSP00000501606.1:p.Asn1149=
ENST00000278616.8:c.3447T>C	ENSP00000278616.4:p.Asn1149=
ENST00000452508.6:c.3447T>C	ENSP00000388058.2:p.Asn1149=
ENST00000527805.5:c.3447T>C	ENSP00000435747.1:p.Asn1149=
NM_000051.3:c.3447T>C , LRG_135t1:c.3447T>C	NP_000042.3:p.Asn1149=
XM_005271561.3:c.3447T>C	XP_005271618.2:p.Asn1149=
XM_005271562.3:c.3447T>C	XP_005271619.2:p.Asn1149=
XM_006718843.2:c.3447T>C	XP_006718906.1:p.Asn1149=
XM_011542840.1:c.3447T>C	XP_011541142.1:p.Asn1149=
XM_011542841.1:c.3447T>C	XP_011541143.1:p.Asn1149=
XM_011542842.1:c.3282T>C	XP_011541144.1:p.Asn1094=
XM_011542843.1:c.3447T>C	XP_011541145.1:p.Asn1149=
XM_011542844.1:c.2403T>C	XP_011541146.1:p.Asn801=
XM_011542845.1:c.2139T>C	XP_011541147.1:p.Asn713=
XM_011542846.1:c.3447T>C	XP_011541148.1:p.Asn1149=
NM_001351834.1:c.3447T>C	NP_001338763.1:p.Asn1149=
XM_005271562.5:c.3447T>C	XP_005271619.2:p.Asn1149=
XM_006718843.4:c.3447T>C	XP_006718906.1:p.Asn1149=
XM_011542840.3:c.3447T>C	XP_011541142.1:p.Asn1149=
XM_011542842.3:c.3282T>C	XP_011541144.1:p.Asn1094=
XM_011542843.2:c.3447T>C	XP_011541145.1:p.Asn1149=
XM_011542844.3:c.2403T>C	XP_011541146.1:p.Asn801=
XM_011542845.2:c.2139T>C	XP_011541147.1:p.Asn713=
XM_017017789.2:c.3447T>C	XP_016873278.1:p.Asn1149=
XM_017017790.2:c.3447T>C	XP_016873279.1:p.Asn1149=
XM_017017791.1:c.3447T>C	XP_016873280.1:p.Asn1149=
XM_017017792.2:c.3447T>C	XP_016873281.1:p.Asn1149=
XR_002957150.1:n.4180T>C
NM_001351834.2:c.3447T>C	NP_001338763.1:p.Asn1149=
NM_000051.4:c.3447T>C MANE Select	NP_000042.3:p.Asn1149=