Canonical Allele Identifier: CA382547732

Gene: ATM

Linked Data

• ClinVar Variation Id: 1720606
• ClinVar RCV Id: RCV002298324 ; RCV002346589
• dbSNP Id: rs2135975734
• MyVariant Identifiers: chr11:g.108178627C>T (hg19) ; chr11:g.108307900C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307900C>T , CM000673.2:g.108307900C>T	GRCh38
NC_000011.9:g.108178627C>T , CM000673.1:g.108178627C>T	GRCh37
NC_000011.8:g.107683837C>T	NCBI36
NG_009830.1:g.90069C>T , LRG_135:g.90069C>T
NG_054724.1:g.166933G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5678C>T	ENSP00000388058.2:p.Ser1893Leu
ENST00000713593.1:c.*5149C>T	ENSP00000518889.1:n.*5149C>T
ENST00000278616.9:c.5678C>T	ENSP00000278616.4:p.Ser1893Leu
ENST00000525056.2:n.97C>T
ENST00000682286.1:n.435C>T
ENST00000682302.1:n.96C>T
ENST00000683174.1:n.7162C>T
ENST00000683524.1:n.902C>T
ENST00000684152.1:n.1392C>T
ENST00000527805.6:c.*742C>T	ENSP00000435747.2:n.*742C>T
ENST00000675595.1:c.*742C>T	ENSP00000502563.1:n.*742C>T
ENST00000675843.1:c.5678C>T MANE Select	ENSP00000501606.1:p.Ser1893Leu
ENST00000278616.8:c.5678C>T	ENSP00000278616.4:p.Ser1893Leu
ENST00000452508.6:c.5678C>T	ENSP00000388058.2:p.Ser1893Leu
ENST00000524792.5:n.1893C>T
ENST00000529588.5:c.187-2260C>T
ENST00000533690.5:n.1082C>T
NM_000051.3:c.5678C>T , LRG_135t1:c.5678C>T	NP_000042.3:p.Ser1893Leu
XM_005271561.3:c.5678C>T	XP_005271618.2:p.Ser1893Leu
XM_005271562.3:c.5678C>T	XP_005271619.2:p.Ser1893Leu
XM_006718843.2:c.5678C>T	XP_006718906.1:p.Ser1893Leu
XM_006718845.1:c.1634C>T	XP_006718908.1:p.Ser545Leu
XM_011542840.1:c.5678C>T	XP_011541142.1:p.Ser1893Leu
XM_011542841.1:c.5678C>T	XP_011541143.1:p.Ser1893Leu
XM_011542842.1:c.5513C>T	XP_011541144.1:p.Ser1838Leu
XM_011542843.1:c.5678C>T	XP_011541145.1:p.Ser1893Leu
XM_011542844.1:c.4634C>T	XP_011541146.1:p.Ser1545Leu
XM_011542845.1:c.4370C>T	XP_011541147.1:p.Ser1457Leu
XM_011542847.1:c.749C>T	XP_011541149.1:p.Ser250Leu
NM_001351834.1:c.5678C>T	NP_001338763.1:p.Ser1893Leu
XM_005271562.5:c.5678C>T	XP_005271619.2:p.Ser1893Leu
XM_006718843.4:c.5678C>T	XP_006718906.1:p.Ser1893Leu
XM_006718845.2:c.1634C>T	XP_006718908.1:p.Ser545Leu
XM_011542840.3:c.5678C>T	XP_011541142.1:p.Ser1893Leu
XM_011542842.3:c.5513C>T	XP_011541144.1:p.Ser1838Leu
XM_011542843.2:c.5678C>T	XP_011541145.1:p.Ser1893Leu
XM_011542844.3:c.4634C>T	XP_011541146.1:p.Ser1545Leu
XM_011542845.2:c.4370C>T	XP_011541147.1:p.Ser1457Leu
XM_017017789.2:c.5678C>T	XP_016873278.1:p.Ser1893Leu
XM_017017790.2:c.5678C>T	XP_016873279.1:p.Ser1893Leu
XM_017017791.1:c.5678C>T	XP_016873280.1:p.Ser1893Leu
XR_002957150.1:n.6278C>T
NM_001351834.2:c.5678C>T	NP_001338763.1:p.Ser1893Leu
NM_000051.4:c.5678C>T MANE Select	NP_000042.3:p.Ser1893Leu