Canonical Allele Identifier: CA1998771484

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108251969_108251971delinsCTT , CM000673.2:g.108251969_108251971delinsCTT	GRCh38
NC_000011.9:g.108122696_108122698delinsCTT , CM000673.1:g.108122696_108122698delinsCTT	GRCh37
NC_000011.8:g.107627906_107627908delinsCTT	NCBI36
NG_009830.1:g.34138_34140delinsCTT , LRG_135:g.34138_34140delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.1740_1742delinsCTT	ENSP00000388058.2:p.Leu580=
ENST00000713593.1:c.*1211_*1213delinsCTT	ENSP00000518889.1:n.*1211_*1213delinsCTT
ENST00000278616.9:c.1740_1742delinsCTT	ENSP00000278616.4:p.Leu580=
ENST00000682516.1:n.1874_1876delinsCTT
ENST00000683174.1:n.1890_1892delinsCTT
ENST00000683605.1:n.1235_1237delinsCTT
ENST00000684037.1:c.*675_*677delinsCTT	ENSP00000508245.1:n.*675_*677delinsCTT
ENST00000684061.1:n.1874_1876delinsCTT
ENST00000527805.6:c.1740_1742delinsCTT	ENSP00000435747.2:p.Leu580=
ENST00000675595.1:c.1575_1577delinsCTT	ENSP00000502563.1:p.Leu525=
ENST00000675843.1:c.1740_1742delinsCTT MANE Select	ENSP00000501606.1:p.Leu580=
ENST00000278616.8:c.1740_1742delinsCTT	ENSP00000278616.4:p.Leu580=
ENST00000452508.6:c.1740_1742delinsCTT	ENSP00000388058.2:p.Leu580=
ENST00000527805.5:c.1740_1742delinsCTT	ENSP00000435747.1:p.Leu580=
NM_000051.3:c.1740_1742delinsCTT , LRG_135t1:c.1740_1742delinsCTT	NP_000042.3:p.Leu580=
XM_005271561.3:c.1740_1742delinsCTT	XP_005271618.2:p.Leu580=
XM_005271562.3:c.1740_1742delinsCTT	XP_005271619.2:p.Leu580=
XM_006718843.2:c.1740_1742delinsCTT	XP_006718906.1:p.Leu580=
XM_011542840.1:c.1740_1742delinsCTT	XP_011541142.1:p.Leu580=
XM_011542841.1:c.1740_1742delinsCTT	XP_011541143.1:p.Leu580=
XM_011542842.1:c.1575_1577delinsCTT	XP_011541144.1:p.Leu525=
XM_011542843.1:c.1740_1742delinsCTT	XP_011541145.1:p.Leu580=
XM_011542844.1:c.696_698delinsCTT	XP_011541146.1:p.Leu232=
XM_011542845.1:c.432_434delinsCTT	XP_011541147.1:p.Leu144=
XM_011542846.1:c.1740_1742delinsCTT	XP_011541148.1:p.Leu580=
NM_001351834.1:c.1740_1742delinsCTT	NP_001338763.1:p.Leu580=
XM_005271562.5:c.1740_1742delinsCTT	XP_005271619.2:p.Leu580=
XM_006718843.4:c.1740_1742delinsCTT	XP_006718906.1:p.Leu580=
XM_011542840.3:c.1740_1742delinsCTT	XP_011541142.1:p.Leu580=
XM_011542842.3:c.1575_1577delinsCTT	XP_011541144.1:p.Leu525=
XM_011542843.2:c.1740_1742delinsCTT	XP_011541145.1:p.Leu580=
XM_011542844.3:c.696_698delinsCTT	XP_011541146.1:p.Leu232=
XM_011542845.2:c.432_434delinsCTT	XP_011541147.1:p.Leu144=
XM_017017789.2:c.1740_1742delinsCTT	XP_016873278.1:p.Leu580=
XM_017017790.2:c.1740_1742delinsCTT	XP_016873279.1:p.Leu580=
XM_017017791.1:c.1740_1742delinsCTT	XP_016873280.1:p.Leu580=
XM_017017792.2:c.1740_1742delinsCTT	XP_016873281.1:p.Leu580=
XR_002957150.1:n.2473_2475delinsCTT
NM_001351834.2:c.1740_1742delinsCTT	NP_001338763.1:p.Leu580=
NM_000051.4:c.1740_1742delinsCTT MANE Select	NP_000042.3:p.Leu580=