Canonical Allele Identifier: CA2573146402

Gene: ATM

Linked Data

• ClinVar Variation Id: 1393301
• ClinVar RCV Id: RCV001882375
• dbSNP Id: rs2135266014

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108247016_108247018del , CM000673.2:g.108247016_108247018del	GRCh38
NC_000011.9:g.108117743_108117745del , CM000673.1:g.108117743_108117745del	GRCh37
NC_000011.8:g.107622953_107622955del	NCBI36
NG_009830.1:g.29185_29187del , LRG_135:g.29185_29187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.954_956del	ENSP00000388058.2:p.Leu319del
ENST00000713593.1:c.*425_*427del	ENSP00000518889.1:n.*425_*427del
ENST00000278616.9:c.954_956del	ENSP00000278616.4:p.Leu319del
ENST00000682516.1:n.1088_1090del
ENST00000682956.1:n.1088_1090del
ENST00000683100.1:n.3301_3303del
ENST00000683174.1:n.1104_1106del
ENST00000683605.1:n.449_451del
ENST00000684037.1:c.954_956del	ENSP00000508245.1:p.Leu319del
ENST00000684061.1:n.1088_1090del
ENST00000684179.1:n.923_925del
ENST00000527805.6:c.954_956del	ENSP00000435747.2:p.Leu319del
ENST00000675595.1:c.789_791del	ENSP00000502563.1:p.Leu264del
ENST00000675843.1:c.954_956del MANE Select	ENSP00000501606.1:p.Leu319del
ENST00000278616.8:c.954_956del	ENSP00000278616.4:p.Leu319del
ENST00000452508.6:c.954_956del	ENSP00000388058.2:p.Leu319del
ENST00000527805.5:c.954_956del	ENSP00000435747.1:p.Leu319del
NM_000051.3:c.954_956del , LRG_135t1:c.954_956del	NP_000042.3:p.Leu319del
XM_005271561.3:c.954_956del	XP_005271618.2:p.Leu319del
XM_005271562.3:c.954_956del	XP_005271619.2:p.Leu319del
XM_006718843.2:c.954_956del	XP_006718906.1:p.Leu319del
XM_011542840.1:c.954_956del	XP_011541142.1:p.Leu319del
XM_011542841.1:c.954_956del	XP_011541143.1:p.Leu319del
XM_011542842.1:c.789_791del	XP_011541144.1:p.Leu264del
XM_011542843.1:c.954_956del	XP_011541145.1:p.Leu319del
XM_011542844.1:c.-91_-89del	XP_011541146.1:n.-91_-89del
XM_011542846.1:c.954_956del	XP_011541148.1:p.Leu319del
NM_001351834.1:c.954_956del	NP_001338763.1:p.Leu319del
XM_005271562.5:c.954_956del	XP_005271619.2:p.Leu319del
XM_006718843.4:c.954_956del	XP_006718906.1:p.Leu319del
XM_011542840.3:c.954_956del	XP_011541142.1:p.Leu319del
XM_011542842.3:c.789_791del	XP_011541144.1:p.Leu264del
XM_011542843.2:c.954_956del	XP_011541145.1:p.Leu319del
XM_011542844.3:c.-91_-89del	XP_011541146.1:n.-91_-89del
XM_017017789.2:c.954_956del	XP_016873278.1:p.Leu319del
XM_017017790.2:c.954_956del	XP_016873279.1:p.Leu319del
XM_017017791.1:c.954_956del	XP_016873280.1:p.Leu319del
XM_017017792.2:c.954_956del	XP_016873281.1:p.Leu319del
XR_002957150.1:n.1687_1689del
NM_001351834.2:c.954_956del	NP_001338763.1:p.Leu319del
NM_000051.4:c.954_956del MANE Select	NP_000042.3:p.Leu319del