Canonical Allele Identifier: CA476671505

Gene: ATM

Linked Data

• dbSNP Id: rs2135264820
• MyVariant Identifiers: chr11:g.108117707A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108246980A>T , CM000673.2:g.108246980A>T	GRCh38
NC_000011.9:g.108117707A>T , CM000673.1:g.108117707A>T	GRCh37
NC_000011.8:g.107622917A>T	NCBI36
NG_009830.1:g.29149A>T , LRG_135:g.29149A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.918A>T	ENSP00000388058.2:p.Thr306=
ENST00000713593.1:c.*389A>T	ENSP00000518889.1:n.*389A>T
ENST00000278616.9:c.918A>T	ENSP00000278616.4:p.Thr306=
ENST00000682516.1:n.1052A>T
ENST00000682956.1:n.1052A>T
ENST00000683100.1:n.3265A>T
ENST00000683174.1:n.1068A>T
ENST00000683605.1:n.413A>T
ENST00000684037.1:c.918A>T	ENSP00000508245.1:p.Thr306=
ENST00000684061.1:n.1052A>T
ENST00000684179.1:n.887A>T
ENST00000527805.6:c.918A>T	ENSP00000435747.2:p.Thr306=
ENST00000675595.1:c.753A>T	ENSP00000502563.1:p.Thr251=
ENST00000675843.1:c.918A>T MANE Select	ENSP00000501606.1:p.Thr306=
ENST00000278616.8:c.918A>T	ENSP00000278616.4:p.Thr306=
ENST00000452508.6:c.918A>T	ENSP00000388058.2:p.Thr306=
ENST00000527805.5:c.918A>T	ENSP00000435747.1:p.Thr306=
NM_000051.3:c.918A>T , LRG_135t1:c.918A>T	NP_000042.3:p.Thr306=
XM_005271561.3:c.918A>T	XP_005271618.2:p.Thr306=
XM_005271562.3:c.918A>T	XP_005271619.2:p.Thr306=
XM_006718843.2:c.918A>T	XP_006718906.1:p.Thr306=
XM_011542840.1:c.918A>T	XP_011541142.1:p.Thr306=
XM_011542841.1:c.918A>T	XP_011541143.1:p.Thr306=
XM_011542842.1:c.753A>T	XP_011541144.1:p.Thr251=
XM_011542843.1:c.918A>T	XP_011541145.1:p.Thr306=
XM_011542844.1:c.-127A>T	XP_011541146.1:n.-127A>T
XM_011542846.1:c.918A>T	XP_011541148.1:p.Thr306=
NM_001351834.1:c.918A>T	NP_001338763.1:p.Thr306=
XM_005271562.5:c.918A>T	XP_005271619.2:p.Thr306=
XM_006718843.4:c.918A>T	XP_006718906.1:p.Thr306=
XM_011542840.3:c.918A>T	XP_011541142.1:p.Thr306=
XM_011542842.3:c.753A>T	XP_011541144.1:p.Thr251=
XM_011542843.2:c.918A>T	XP_011541145.1:p.Thr306=
XM_011542844.3:c.-127A>T	XP_011541146.1:n.-127A>T
XM_017017789.2:c.918A>T	XP_016873278.1:p.Thr306=
XM_017017790.2:c.918A>T	XP_016873279.1:p.Thr306=
XM_017017791.1:c.918A>T	XP_016873280.1:p.Thr306=
XM_017017792.2:c.918A>T	XP_016873281.1:p.Thr306=
XR_002957150.1:n.1651A>T
NM_001351834.2:c.918A>T	NP_001338763.1:p.Thr306=
NM_000051.4:c.918A>T MANE Select	NP_000042.3:p.Thr306=