Canonical Allele Identifier: CA1998770779

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108250752_108250754delinsCTG , CM000673.2:g.108250752_108250754delinsCTG	GRCh38
NC_000011.9:g.108121479_108121481delinsCTG , CM000673.1:g.108121479_108121481delinsCTG	GRCh37
NC_000011.8:g.107626689_107626691delinsCTG	NCBI36
NG_009830.1:g.32921_32923delinsCTG , LRG_135:g.32921_32923delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1287_1289delinsCTG	ENSP00000388058.2:p.Asn429=
ENST00000713593.1:c.*758_*760delinsCTG	ENSP00000518889.1:n.*758_*760delinsCTG
ENST00000278616.9:c.1287_1289delinsCTG	ENSP00000278616.4:p.Asn429=
ENST00000682516.1:n.1421_1423delinsCTG
ENST00000682956.1:n.1421_1423delinsCTG
ENST00000683174.1:n.1437_1439delinsCTG
ENST00000683605.1:n.782_784delinsCTG
ENST00000684037.1:c.*222_*224delinsCTG	ENSP00000508245.1:n.*222_*224delinsCTG
ENST00000684061.1:n.1421_1423delinsCTG
ENST00000684179.1:n.1256_1258delinsCTG
ENST00000527805.6:c.1287_1289delinsCTG	ENSP00000435747.2:p.Asn429=
ENST00000675595.1:c.1122_1124delinsCTG	ENSP00000502563.1:p.Asn374=
ENST00000675843.1:c.1287_1289delinsCTG MANE Select	ENSP00000501606.1:p.Asn429=
ENST00000278616.8:c.1287_1289delinsCTG	ENSP00000278616.4:p.Asn429=
ENST00000452508.6:c.1287_1289delinsCTG	ENSP00000388058.2:p.Asn429=
ENST00000527805.5:c.1287_1289delinsCTG	ENSP00000435747.1:p.Asn429=
NM_000051.3:c.1287_1289delinsCTG , LRG_135t1:c.1287_1289delinsCTG	NP_000042.3:p.Asn429=
XM_005271561.3:c.1287_1289delinsCTG	XP_005271618.2:p.Asn429=
XM_005271562.3:c.1287_1289delinsCTG	XP_005271619.2:p.Asn429=
XM_006718843.2:c.1287_1289delinsCTG	XP_006718906.1:p.Asn429=
XM_011542840.1:c.1287_1289delinsCTG	XP_011541142.1:p.Asn429=
XM_011542841.1:c.1287_1289delinsCTG	XP_011541143.1:p.Asn429=
XM_011542842.1:c.1122_1124delinsCTG	XP_011541144.1:p.Asn374=
XM_011542843.1:c.1287_1289delinsCTG	XP_011541145.1:p.Asn429=
XM_011542844.1:c.243_245delinsCTG	XP_011541146.1:p.Asn81=
XM_011542845.1:c.-22_-20delinsCTG	XP_011541147.1:n.-22_-20delinsCTG
XM_011542846.1:c.1287_1289delinsCTG	XP_011541148.1:p.Asn429=
NM_001351834.1:c.1287_1289delinsCTG	NP_001338763.1:p.Asn429=
XM_005271562.5:c.1287_1289delinsCTG	XP_005271619.2:p.Asn429=
XM_006718843.4:c.1287_1289delinsCTG	XP_006718906.1:p.Asn429=
XM_011542840.3:c.1287_1289delinsCTG	XP_011541142.1:p.Asn429=
XM_011542842.3:c.1122_1124delinsCTG	XP_011541144.1:p.Asn374=
XM_011542843.2:c.1287_1289delinsCTG	XP_011541145.1:p.Asn429=
XM_011542844.3:c.243_245delinsCTG	XP_011541146.1:p.Asn81=
XM_011542845.2:c.-22_-20delinsCTG	XP_011541147.1:n.-22_-20delinsCTG
XM_017017789.2:c.1287_1289delinsCTG	XP_016873278.1:p.Asn429=
XM_017017790.2:c.1287_1289delinsCTG	XP_016873279.1:p.Asn429=
XM_017017791.1:c.1287_1289delinsCTG	XP_016873280.1:p.Asn429=
XM_017017792.2:c.1287_1289delinsCTG	XP_016873281.1:p.Asn429=
XR_002957150.1:n.2020_2022delinsCTG
NM_001351834.2:c.1287_1289delinsCTG	NP_001338763.1:p.Asn429=
NM_000051.4:c.1287_1289delinsCTG MANE Select	NP_000042.3:p.Asn429=