Canonical Allele Identifier: CA1998795410

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108287621_108287632delinsAATTTACCAGAG , CM000673.2:g.108287621_108287632delinsAATTTACCAGAG	GRCh38
NC_000011.9:g.108158348_108158359delinsAATTTACCAGAG , CM000673.1:g.108158348_108158359delinsAATTTACCAGAG	GRCh37
NC_000011.8:g.107663558_107663569delinsAATTTACCAGAG	NCBI36
NG_009830.1:g.69790_69801delinsAATTTACCAGAG , LRG_135:g.69790_69801delinsAATTTACCAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4015_4026delinsAATTTACCAGAG	ENSP00000388058.2:p.Asn1339=
ENST00000713593.1:c.*3486_*3497delinsAATTTACCAGAG	ENSP00000518889.1:n.*3486_*3497delinsAATTTACCAGAG
ENST00000278616.9:c.4015_4026delinsAATTTACCAGAG	ENSP00000278616.4:p.Asn1339=
ENST00000533733.6:n.1278_1289delinsAATTTACCAGAG
ENST00000683174.1:n.4165_4176delinsAATTTACCAGAG
ENST00000527805.6:c.4015_4026delinsAATTTACCAGAG	ENSP00000435747.2:p.Asn1339=
ENST00000675595.1:c.3850_3861delinsAATTTACCAGAG	ENSP00000502563.1:p.Asn1284=
ENST00000675843.1:c.4015_4026delinsAATTTACCAGAG MANE Select	ENSP00000501606.1:p.Asn1339=
ENST00000278616.8:c.4015_4026delinsAATTTACCAGAG	ENSP00000278616.4:p.Asn1339=
ENST00000452508.6:c.4015_4026delinsAATTTACCAGAG	ENSP00000388058.2:p.Asn1339=
ENST00000524792.5:n.230_241delinsAATTTACCAGAG
ENST00000527805.5:c.4015_4026delinsAATTTACCAGAG	ENSP00000435747.1:p.Asn1339=
ENST00000531525.2:c.22_33delinsAATTTACCAGAG	ENSP00000434327.2:p.Asn8=
ENST00000533733.5:n.444_455delinsAATTTACCAGAG
NM_000051.3:c.4015_4026delinsAATTTACCAGAG , LRG_135t1:c.4015_4026delinsAATTTACCAGAG	NP_000042.3:p.Asn1339=
XM_005271561.3:c.4015_4026delinsAATTTACCAGAG	XP_005271618.2:p.Asn1339=
XM_005271562.3:c.4015_4026delinsAATTTACCAGAG	XP_005271619.2:p.Asn1339=
XM_006718843.2:c.4015_4026delinsAATTTACCAGAG	XP_006718906.1:p.Asn1339=
XM_006718845.1:c.-30_-19delinsAATTTACCAGAG	XP_006718908.1:n.-30_-19delinsAATTTACCAGAG
XM_011542840.1:c.4015_4026delinsAATTTACCAGAG	XP_011541142.1:p.Asn1339=
XM_011542841.1:c.4015_4026delinsAATTTACCAGAG	XP_011541143.1:p.Asn1339=
XM_011542842.1:c.3850_3861delinsAATTTACCAGAG	XP_011541144.1:p.Asn1284=
XM_011542843.1:c.4015_4026delinsAATTTACCAGAG	XP_011541145.1:p.Asn1339=
XM_011542844.1:c.2971_2982delinsAATTTACCAGAG	XP_011541146.1:p.Asn991=
XM_011542845.1:c.2707_2718delinsAATTTACCAGAG	XP_011541147.1:p.Asn903=
XM_011542846.1:c.4015_4026delinsAATTTACCAGAG	XP_011541148.1:p.Asn1339=
NM_001351834.1:c.4015_4026delinsAATTTACCAGAG	NP_001338763.1:p.Asn1339=
XM_005271562.5:c.4015_4026delinsAATTTACCAGAG	XP_005271619.2:p.Asn1339=
XM_006718843.4:c.4015_4026delinsAATTTACCAGAG	XP_006718906.1:p.Asn1339=
XM_006718845.2:c.-30_-19delinsAATTTACCAGAG	XP_006718908.1:n.-30_-19delinsAATTTACCAGAG
XM_011542840.3:c.4015_4026delinsAATTTACCAGAG	XP_011541142.1:p.Asn1339=
XM_011542842.3:c.3850_3861delinsAATTTACCAGAG	XP_011541144.1:p.Asn1284=
XM_011542843.2:c.4015_4026delinsAATTTACCAGAG	XP_011541145.1:p.Asn1339=
XM_011542844.3:c.2971_2982delinsAATTTACCAGAG	XP_011541146.1:p.Asn991=
XM_011542845.2:c.2707_2718delinsAATTTACCAGAG	XP_011541147.1:p.Asn903=
XM_017017789.2:c.4015_4026delinsAATTTACCAGAG	XP_016873278.1:p.Asn1339=
XM_017017790.2:c.4015_4026delinsAATTTACCAGAG	XP_016873279.1:p.Asn1339=
XM_017017791.1:c.4015_4026delinsAATTTACCAGAG	XP_016873280.1:p.Asn1339=
XM_017017792.2:c.4015_4026delinsAATTTACCAGAG	XP_016873281.1:p.Asn1339=
XR_002957150.1:n.4748_4759delinsAATTTACCAGAG
NM_001351834.2:c.4015_4026delinsAATTTACCAGAG	NP_001338763.1:p.Asn1339=
NM_000051.4:c.4015_4026delinsAATTTACCAGAG MANE Select	NP_000042.3:p.Asn1339=