Canonical Allele Identifier: CA382544164

Gene: ATM

Linked Data

• dbSNP Id: rs2083505400
• MyVariant Identifiers: chr11:g.108173702G>T (hg19) ; chr11:g.108302975G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108302975G>T , CM000673.2:g.108302975G>T	GRCh38
NC_000011.9:g.108173702G>T , CM000673.1:g.108173702G>T	GRCh37
NC_000011.8:g.107678912G>T	NCBI36
NG_009830.1:g.85144G>T , LRG_135:g.85144G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5442G>T	ENSP00000388058.2:p.Leu1814Phe
ENST00000713593.1:c.*4913G>T	ENSP00000518889.1:n.*4913G>T
ENST00000278616.9:c.5442G>T	ENSP00000278616.4:p.Leu1814Phe
ENST00000683174.1:n.6926G>T
ENST00000683524.1:n.666G>T
ENST00000684152.1:n.1156G>T
ENST00000527805.6:c.*506G>T	ENSP00000435747.2:n.*506G>T
ENST00000675595.1:c.*506G>T	ENSP00000502563.1:n.*506G>T
ENST00000675843.1:c.5442G>T MANE Select	ENSP00000501606.1:p.Leu1814Phe
ENST00000278616.8:c.5442G>T	ENSP00000278616.4:p.Leu1814Phe
ENST00000452508.6:c.5442G>T	ENSP00000388058.2:p.Leu1814Phe
ENST00000524792.5:n.1657G>T
ENST00000533690.5:n.846G>T
ENST00000534625.1:n.671G>T
NM_000051.3:c.5442G>T , LRG_135t1:c.5442G>T	NP_000042.3:p.Leu1814Phe
XM_005271561.3:c.5442G>T	XP_005271618.2:p.Leu1814Phe
XM_005271562.3:c.5442G>T	XP_005271619.2:p.Leu1814Phe
XM_006718843.2:c.5442G>T	XP_006718906.1:p.Leu1814Phe
XM_006718845.1:c.1398G>T	XP_006718908.1:p.Leu466Phe
XM_011542840.1:c.5442G>T	XP_011541142.1:p.Leu1814Phe
XM_011542841.1:c.5442G>T	XP_011541143.1:p.Leu1814Phe
XM_011542842.1:c.5277G>T	XP_011541144.1:p.Leu1759Phe
XM_011542843.1:c.5442G>T	XP_011541145.1:p.Leu1814Phe
XM_011542844.1:c.4398G>T	XP_011541146.1:p.Leu1466Phe
XM_011542845.1:c.4134G>T	XP_011541147.1:p.Leu1378Phe
XM_011542847.1:c.513G>T	XP_011541149.1:p.Leu171Phe
NM_001351834.1:c.5442G>T	NP_001338763.1:p.Leu1814Phe
XM_005271562.5:c.5442G>T	XP_005271619.2:p.Leu1814Phe
XM_006718843.4:c.5442G>T	XP_006718906.1:p.Leu1814Phe
XM_006718845.2:c.1398G>T	XP_006718908.1:p.Leu466Phe
XM_011542840.3:c.5442G>T	XP_011541142.1:p.Leu1814Phe
XM_011542842.3:c.5277G>T	XP_011541144.1:p.Leu1759Phe
XM_011542843.2:c.5442G>T	XP_011541145.1:p.Leu1814Phe
XM_011542844.3:c.4398G>T	XP_011541146.1:p.Leu1466Phe
XM_011542845.2:c.4134G>T	XP_011541147.1:p.Leu1378Phe
XM_017017789.2:c.5442G>T	XP_016873278.1:p.Leu1814Phe
XM_017017790.2:c.5442G>T	XP_016873279.1:p.Leu1814Phe
XM_017017791.1:c.5442G>T	XP_016873280.1:p.Leu1814Phe
XR_002957150.1:n.6042G>T
NM_001351834.2:c.5442G>T	NP_001338763.1:p.Leu1814Phe
NM_000051.4:c.5442G>T MANE Select	NP_000042.3:p.Leu1814Phe