Canonical Allele Identifier: CA671413516

Gene: ATM

Linked Data

• dbSNP Id: rs1180212165
• MyVariant Identifiers: chr11:g.108173554A>C (hg19) ; chr11:g.108302827A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108302827A>C , CM000673.2:g.108302827A>C	GRCh38
NC_000011.9:g.108173554A>C , CM000673.1:g.108173554A>C	GRCh37
NC_000011.8:g.107678764A>C	NCBI36
NG_009830.1:g.84996A>C , LRG_135:g.84996A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.5320-26A>C	ENSP00000388058.2:n.5320-26A>C
ENST00000713593.1:c.*4791-26A>C	ENSP00000518889.1:n.*4791-26A>C
ENST00000278616.9:c.5320-26A>C	ENSP00000278616.4:n.5320-26A>C
ENST00000683174.1:n.6804-26A>C
ENST00000683524.1:n.544-26A>C
ENST00000684152.1:n.1034-26A>C
ENST00000527805.6:c.*384-26A>C	ENSP00000435747.2:n.*384-26A>C
ENST00000675595.1:c.*384-26A>C	ENSP00000502563.1:n.*384-26A>C
ENST00000675843.1:c.5320-26A>C MANE Select	ENSP00000501606.1:n.5320-26A>C
ENST00000278616.8:c.5320-26A>C	ENSP00000278616.4:n.5320-26A>C
ENST00000452508.6:c.5320-26A>C	ENSP00000388058.2:n.5320-26A>C
ENST00000524792.5:n.1535-26A>C
ENST00000533690.5:n.724-26A>C
ENST00000534625.1:n.549-26A>C
NM_000051.3:c.5320-26A>C , LRG_135t1:c.5320-26A>C	NP_000042.3:n.5320-26A>C
XM_005271561.3:c.5320-26A>C	XP_005271618.2:n.5320-26A>C
XM_005271562.3:c.5320-26A>C	XP_005271619.2:n.5320-26A>C
XM_006718843.2:c.5320-26A>C	XP_006718906.1:n.5320-26A>C
XM_006718845.1:c.1276-26A>C	XP_006718908.1:n.1276-26A>C
XM_011542840.1:c.5320-26A>C	XP_011541142.1:n.5320-26A>C
XM_011542841.1:c.5320-26A>C	XP_011541143.1:n.5320-26A>C
XM_011542842.1:c.5155-26A>C	XP_011541144.1:n.5155-26A>C
XM_011542843.1:c.5320-26A>C	XP_011541145.1:n.5320-26A>C
XM_011542844.1:c.4276-26A>C	XP_011541146.1:n.4276-26A>C
XM_011542845.1:c.4012-26A>C	XP_011541147.1:n.4012-26A>C
XM_011542846.1:c.5319-24A>C	XP_011541148.1:n.5319-24A>C
XM_011542847.1:c.391-26A>C	XP_011541149.1:n.391-26A>C
NM_001351834.1:c.5320-26A>C	NP_001338763.1:n.5320-26A>C
XM_005271562.5:c.5320-26A>C	XP_005271619.2:n.5320-26A>C
XM_006718843.4:c.5320-26A>C	XP_006718906.1:n.5320-26A>C
XM_006718845.2:c.1276-26A>C	XP_006718908.1:n.1276-26A>C
XM_011542840.3:c.5320-26A>C	XP_011541142.1:n.5320-26A>C
XM_011542842.3:c.5155-26A>C	XP_011541144.1:n.5155-26A>C
XM_011542843.2:c.5320-26A>C	XP_011541145.1:n.5320-26A>C
XM_011542844.3:c.4276-26A>C	XP_011541146.1:n.4276-26A>C
XM_011542845.2:c.4012-26A>C	XP_011541147.1:n.4012-26A>C
XM_017017789.2:c.5320-26A>C	XP_016873278.1:n.5320-26A>C
XM_017017790.2:c.5320-26A>C	XP_016873279.1:n.5320-26A>C
XM_017017791.1:c.5320-26A>C	XP_016873280.1:n.5320-26A>C
XM_017017792.2:c.*1-26A>C	XP_016873281.1:n.*1-26A>C
XR_002957150.1:n.5920-26A>C
NM_001351834.2:c.5320-26A>C	NP_001338763.1:n.5320-26A>C
NM_000051.4:c.5320-26A>C MANE Select	NP_000042.3:n.5320-26A>C