Canonical Allele Identifier: CA382524660

Gene: ATM

Linked Data

• ClinVar Variation Id: 1350539
• ClinVar RCV Id: RCV002041939
• dbSNP Id: rs2135705400
• MyVariant Identifiers: chr11:g.108155003G>C (hg19) ; chr11:g.108284276G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108284276G>C , CM000673.2:g.108284276G>C	GRCh38
NC_000011.9:g.108155003G>C , CM000673.1:g.108155003G>C	GRCh37
NC_000011.8:g.107660213G>C	NCBI36
NG_009830.1:g.66445G>C , LRG_135:g.66445G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.3796G>C	ENSP00000388058.2:p.Asp1266His
ENST00000713593.1:c.*3267G>C	ENSP00000518889.1:n.*3267G>C
ENST00000278616.9:c.3796G>C	ENSP00000278616.4:p.Asp1266His
ENST00000682289.1:n.143G>C
ENST00000683174.1:n.3946G>C
ENST00000527805.6:c.3796G>C	ENSP00000435747.2:p.Asp1266His
ENST00000675595.1:c.3631G>C	ENSP00000502563.1:p.Asp1211His
ENST00000675843.1:c.3796G>C MANE Select	ENSP00000501606.1:p.Asp1266His
ENST00000278616.8:c.3796G>C	ENSP00000278616.4:p.Asp1266His
ENST00000452508.6:c.3796G>C	ENSP00000388058.2:p.Asp1266His
ENST00000527805.5:c.3796G>C	ENSP00000435747.1:p.Asp1266His
NM_000051.3:c.3796G>C , LRG_135t1:c.3796G>C	NP_000042.3:p.Asp1266His
XM_005271561.3:c.3796G>C	XP_005271618.2:p.Asp1266His
XM_005271562.3:c.3796G>C	XP_005271619.2:p.Asp1266His
XM_006718843.2:c.3796G>C	XP_006718906.1:p.Asp1266His
XM_011542840.1:c.3796G>C	XP_011541142.1:p.Asp1266His
XM_011542841.1:c.3796G>C	XP_011541143.1:p.Asp1266His
XM_011542842.1:c.3631G>C	XP_011541144.1:p.Asp1211His
XM_011542843.1:c.3796G>C	XP_011541145.1:p.Asp1266His
XM_011542844.1:c.2752G>C	XP_011541146.1:p.Asp918His
XM_011542845.1:c.2488G>C	XP_011541147.1:p.Asp830His
XM_011542846.1:c.3796G>C	XP_011541148.1:p.Asp1266His
NM_001351834.1:c.3796G>C	NP_001338763.1:p.Asp1266His
XM_005271562.5:c.3796G>C	XP_005271619.2:p.Asp1266His
XM_006718843.4:c.3796G>C	XP_006718906.1:p.Asp1266His
XM_011542840.3:c.3796G>C	XP_011541142.1:p.Asp1266His
XM_011542842.3:c.3631G>C	XP_011541144.1:p.Asp1211His
XM_011542843.2:c.3796G>C	XP_011541145.1:p.Asp1266His
XM_011542844.3:c.2752G>C	XP_011541146.1:p.Asp918His
XM_011542845.2:c.2488G>C	XP_011541147.1:p.Asp830His
XM_017017789.2:c.3796G>C	XP_016873278.1:p.Asp1266His
XM_017017790.2:c.3796G>C	XP_016873279.1:p.Asp1266His
XM_017017791.1:c.3796G>C	XP_016873280.1:p.Asp1266His
XM_017017792.2:c.3796G>C	XP_016873281.1:p.Asp1266His
XR_002957150.1:n.4529G>C
NM_001351834.2:c.3796G>C	NP_001338763.1:p.Asp1266His
NM_000051.4:c.3796G>C MANE Select	NP_000042.3:p.Asp1266His