Canonical Allele Identifier: CA1998765399

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108245039_108245040delinsTG , CM000673.2:g.108245039_108245040delinsTG	GRCh38
NC_000011.9:g.108115766_108115767delinsTG , CM000673.1:g.108115766_108115767delinsTG	GRCh37
NC_000011.8:g.107620976_107620977delinsTG	NCBI36
NG_009830.1:g.27208_27209delinsTG , LRG_135:g.27208_27209delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.901+13_901+14delinsTG	ENSP00000388058.2:n.901+13_901+14delinsTG
ENST00000713593.1:c.*372+13_*372+14delinsTG	ENSP00000518889.1:n.*372+13_*372+14delinsTG
ENST00000278616.9:c.901+13_901+14delinsTG	ENSP00000278616.4:n.901+13_901+14delinsTG
ENST00000682516.1:n.1035+13_1035+14delinsTG
ENST00000682956.1:n.1035+13_1035+14delinsTG
ENST00000683100.1:n.3248+13_3248+14delinsTG
ENST00000683174.1:n.1051+13_1051+14delinsTG
ENST00000683605.1:n.396+13_396+14delinsTG
ENST00000684037.1:c.901+13_901+14delinsTG	ENSP00000508245.1:n.901+13_901+14delinsTG
ENST00000684061.1:n.1035+13_1035+14delinsTG
ENST00000684179.1:n.870+13_870+14delinsTG
ENST00000527805.6:c.901+13_901+14delinsTG	ENSP00000435747.2:n.901+13_901+14delinsTG
ENST00000675595.1:c.736+13_736+14delinsTG	ENSP00000502563.1:n.736+13_736+14delinsTG
ENST00000675843.1:c.901+13_901+14delinsTG MANE Select	ENSP00000501606.1:n.901+13_901+14delinsTG
ENST00000278616.8:c.901+13_901+14delinsTG	ENSP00000278616.4:n.901+13_901+14delinsTG
ENST00000452508.6:c.901+13_901+14delinsTG	ENSP00000388058.2:n.901+13_901+14delinsTG
ENST00000527805.5:c.901+13_901+14delinsTG	ENSP00000435747.1:n.901+13_901+14delinsTG
NM_000051.3:c.901+13_901+14delinsTG , LRG_135t1:c.901+13_901+14delinsTG	NP_000042.3:n.901+13_901+14delinsTG
XM_005271561.3:c.901+13_901+14delinsTG	XP_005271618.2:n.901+13_901+14delinsTG
XM_005271562.3:c.901+13_901+14delinsTG	XP_005271619.2:n.901+13_901+14delinsTG
XM_006718843.2:c.901+13_901+14delinsTG	XP_006718906.1:n.901+13_901+14delinsTG
XM_011542840.1:c.901+13_901+14delinsTG	XP_011541142.1:n.901+13_901+14delinsTG
XM_011542841.1:c.901+13_901+14delinsTG	XP_011541143.1:n.901+13_901+14delinsTG
XM_011542842.1:c.736+13_736+14delinsTG	XP_011541144.1:n.736+13_736+14delinsTG
XM_011542843.1:c.901+13_901+14delinsTG	XP_011541145.1:n.901+13_901+14delinsTG
XM_011542844.1:c.-144+13_-144+14delinsTG	XP_011541146.1:n.-144+13_-144+14delinsTG
XM_011542846.1:c.901+13_901+14delinsTG	XP_011541148.1:n.901+13_901+14delinsTG
NM_001351834.1:c.901+13_901+14delinsTG	NP_001338763.1:n.901+13_901+14delinsTG
XM_005271562.5:c.901+13_901+14delinsTG	XP_005271619.2:n.901+13_901+14delinsTG
XM_006718843.4:c.901+13_901+14delinsTG	XP_006718906.1:n.901+13_901+14delinsTG
XM_011542840.3:c.901+13_901+14delinsTG	XP_011541142.1:n.901+13_901+14delinsTG
XM_011542842.3:c.736+13_736+14delinsTG	XP_011541144.1:n.736+13_736+14delinsTG
XM_011542843.2:c.901+13_901+14delinsTG	XP_011541145.1:n.901+13_901+14delinsTG
XM_011542844.3:c.-144+13_-144+14delinsTG	XP_011541146.1:n.-144+13_-144+14delinsTG
XM_017017789.2:c.901+13_901+14delinsTG	XP_016873278.1:n.901+13_901+14delinsTG
XM_017017790.2:c.901+13_901+14delinsTG	XP_016873279.1:n.901+13_901+14delinsTG
XM_017017791.1:c.901+13_901+14delinsTG	XP_016873280.1:n.901+13_901+14delinsTG
XM_017017792.2:c.901+13_901+14delinsTG	XP_016873281.1:n.901+13_901+14delinsTG
XR_002957150.1:n.1634+13_1634+14delinsTG
NM_001351834.2:c.901+13_901+14delinsTG	NP_001338763.1:n.901+13_901+14delinsTG
NM_000051.4:c.901+13_901+14delinsTG MANE Select	NP_000042.3:n.901+13_901+14delinsTG