Canonical Allele Identifier: CA382545574

Gene: ATM

Linked Data

• ClinVar Variation Id: 849722
• ClinVar RCV Id: RCV001053747
• dbSNP Id: rs2081392000
• MyVariant Identifiers: chr11:g.108139281T>C (hg19) ; chr11:g.108268554T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108268554T>C , CM000673.2:g.108268554T>C	GRCh38
NC_000011.9:g.108139281T>C , CM000673.1:g.108139281T>C	GRCh37
NC_000011.8:g.107644491T>C	NCBI36
NG_009830.1:g.50723T>C , LRG_135:g.50723T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.2783T>C	ENSP00000388058.2:p.Leu928Ser
ENST00000713593.1:c.*2254T>C	ENSP00000518889.1:n.*2254T>C
ENST00000278616.9:c.2783T>C	ENSP00000278616.4:p.Leu928Ser
ENST00000682516.1:n.2772+1212T>C
ENST00000683174.1:n.2933T>C
ENST00000684037.1:c.*1573+1212T>C	ENSP00000508245.1:n.*1573+1212T>C
ENST00000527805.6:c.2783T>C	ENSP00000435747.2:p.Leu928Ser
ENST00000675595.1:c.2618T>C	ENSP00000502563.1:p.Leu873Ser
ENST00000675843.1:c.2783T>C MANE Select	ENSP00000501606.1:p.Leu928Ser
ENST00000278616.8:c.2783T>C	ENSP00000278616.4:p.Leu928Ser
ENST00000419286.2:n.145T>C
ENST00000452508.6:c.2783T>C	ENSP00000388058.2:p.Leu928Ser
ENST00000527805.5:c.2783T>C	ENSP00000435747.1:p.Leu928Ser
NM_000051.3:c.2783T>C , LRG_135t1:c.2783T>C	NP_000042.3:p.Leu928Ser
XM_005271561.3:c.2783T>C	XP_005271618.2:p.Leu928Ser
XM_005271562.3:c.2783T>C	XP_005271619.2:p.Leu928Ser
XM_006718843.2:c.2783T>C	XP_006718906.1:p.Leu928Ser
XM_011542840.1:c.2783T>C	XP_011541142.1:p.Leu928Ser
XM_011542841.1:c.2783T>C	XP_011541143.1:p.Leu928Ser
XM_011542842.1:c.2618T>C	XP_011541144.1:p.Leu873Ser
XM_011542843.1:c.2783T>C	XP_011541145.1:p.Leu928Ser
XM_011542844.1:c.1739T>C	XP_011541146.1:p.Leu580Ser
XM_011542845.1:c.1475T>C	XP_011541147.1:p.Leu492Ser
XM_011542846.1:c.2783T>C	XP_011541148.1:p.Leu928Ser
NM_001351834.1:c.2783T>C	NP_001338763.1:p.Leu928Ser
XM_005271562.5:c.2783T>C	XP_005271619.2:p.Leu928Ser
XM_006718843.4:c.2783T>C	XP_006718906.1:p.Leu928Ser
XM_011542840.3:c.2783T>C	XP_011541142.1:p.Leu928Ser
XM_011542842.3:c.2618T>C	XP_011541144.1:p.Leu873Ser
XM_011542843.2:c.2783T>C	XP_011541145.1:p.Leu928Ser
XM_011542844.3:c.1739T>C	XP_011541146.1:p.Leu580Ser
XM_011542845.2:c.1475T>C	XP_011541147.1:p.Leu492Ser
XM_017017789.2:c.2783T>C	XP_016873278.1:p.Leu928Ser
XM_017017790.2:c.2783T>C	XP_016873279.1:p.Leu928Ser
XM_017017791.1:c.2783T>C	XP_016873280.1:p.Leu928Ser
XM_017017792.2:c.2783T>C	XP_016873281.1:p.Leu928Ser
XR_002957150.1:n.3516T>C
NM_001351834.2:c.2783T>C	NP_001338763.1:p.Leu928Ser
NM_000051.4:c.2783T>C MANE Select	NP_000042.3:p.Leu928Ser