Canonical Allele Identifier: CA382547938

Gene: ATM

Linked Data

• MyVariant Identifiers: chr11:g.108178670A>C (hg19) ; chr11:g.108307943A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307943A>C , CM000673.2:g.108307943A>C	GRCh38
NC_000011.9:g.108178670A>C , CM000673.1:g.108178670A>C	GRCh37
NC_000011.8:g.107683880A>C	NCBI36
NG_009830.1:g.90112A>C , LRG_135:g.90112A>C
NG_054724.1:g.166890T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.5721A>C	ENSP00000388058.2:p.Arg1907Ser
ENST00000713593.1:c.*5192A>C	ENSP00000518889.1:n.*5192A>C
ENST00000278616.9:c.5721A>C	ENSP00000278616.4:p.Arg1907Ser
ENST00000525056.2:n.140A>C
ENST00000682286.1:n.478A>C
ENST00000682302.1:n.139A>C
ENST00000683174.1:n.7205A>C
ENST00000683524.1:n.945A>C
ENST00000684152.1:n.1435A>C
ENST00000527805.6:c.*785A>C	ENSP00000435747.2:n.*785A>C
ENST00000675595.1:c.*785A>C	ENSP00000502563.1:n.*785A>C
ENST00000675843.1:c.5721A>C MANE Select	ENSP00000501606.1:p.Arg1907Ser
ENST00000278616.8:c.5721A>C	ENSP00000278616.4:p.Arg1907Ser
ENST00000452508.6:c.5721A>C	ENSP00000388058.2:p.Arg1907Ser
ENST00000524792.5:n.1936A>C
ENST00000529588.5:c.187-2217A>C
ENST00000533690.5:n.1125A>C
NM_000051.3:c.5721A>C , LRG_135t1:c.5721A>C	NP_000042.3:p.Arg1907Ser
XM_005271561.3:c.5721A>C	XP_005271618.2:p.Arg1907Ser
XM_005271562.3:c.5721A>C	XP_005271619.2:p.Arg1907Ser
XM_006718843.2:c.5721A>C	XP_006718906.1:p.Arg1907Ser
XM_006718845.1:c.1677A>C	XP_006718908.1:p.Arg559Ser
XM_011542840.1:c.5721A>C	XP_011541142.1:p.Arg1907Ser
XM_011542841.1:c.5721A>C	XP_011541143.1:p.Arg1907Ser
XM_011542842.1:c.5556A>C	XP_011541144.1:p.Arg1852Ser
XM_011542843.1:c.5721A>C	XP_011541145.1:p.Arg1907Ser
XM_011542844.1:c.4677A>C	XP_011541146.1:p.Arg1559Ser
XM_011542845.1:c.4413A>C	XP_011541147.1:p.Arg1471Ser
XM_011542847.1:c.792A>C	XP_011541149.1:p.Arg264Ser
NM_001351834.1:c.5721A>C	NP_001338763.1:p.Arg1907Ser
XM_005271562.5:c.5721A>C	XP_005271619.2:p.Arg1907Ser
XM_006718843.4:c.5721A>C	XP_006718906.1:p.Arg1907Ser
XM_006718845.2:c.1677A>C	XP_006718908.1:p.Arg559Ser
XM_011542840.3:c.5721A>C	XP_011541142.1:p.Arg1907Ser
XM_011542842.3:c.5556A>C	XP_011541144.1:p.Arg1852Ser
XM_011542843.2:c.5721A>C	XP_011541145.1:p.Arg1907Ser
XM_011542844.3:c.4677A>C	XP_011541146.1:p.Arg1559Ser
XM_011542845.2:c.4413A>C	XP_011541147.1:p.Arg1471Ser
XM_017017789.2:c.5721A>C	XP_016873278.1:p.Arg1907Ser
XM_017017790.2:c.5721A>C	XP_016873279.1:p.Arg1907Ser
XM_017017791.1:c.5721A>C	XP_016873280.1:p.Arg1907Ser
XR_002957150.1:n.6321A>C
NM_001351834.2:c.5721A>C	NP_001338763.1:p.Arg1907Ser
NM_000051.4:c.5721A>C MANE Select	NP_000042.3:p.Arg1907Ser