Canonical Allele Identifier: CA10579189
Community Standard Title: NM_000051.4(ATM):c.5631_5635delinsA (p.Phe1877LeufsTer?)
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108304809_108304813delinsA , CM000673.2:g.108304809_108304813delinsA GRCh38
NC_000011.9:g.108175536_108175540delinsA , CM000673.1:g.108175536_108175540delinsA GRCh37
NC_000011.8:g.107680746_107680750delinsA NCBI36
NG_009830.1:g.86978_86982delinsA , LRG_135:g.86978_86982delinsA

Transcript Alleles

HGVS Amino-acid Change
NM_000051.4:c.5631_5635delinsA MANE Select NP_000042.3:p.Phe1877LeufsTer?
ENST00000675843.1:c.5631_5635delinsA MANE Select ENSP00000501606.1:p.Phe1877LeufsTer?
NM_000051.3:c.5631_5635delinsA , LRG_135t1:c.5631_5635delinsA NP_000042.3:p.Phe1877LeufsTer?
NM_001351834.1:c.5631_5635delinsA NP_001338763.1:p.Phe1877LeufsTer?
NM_001351834.2:c.5631_5635delinsA NP_001338763.1:p.Phe1877LeufsTer?
ENST00000278616.8:c.5631_5635delinsA ENSP00000278616.4:p.Phe1877LeufsTer?
ENST00000278616.9:c.5631_5635delinsA ENSP00000278616.4:p.Phe1877LeufsTer?
ENST00000452508.6:c.5631_5635delinsA ENSP00000388058.2:p.Phe1877LeufsTer?
ENST00000452508.7:c.5631_5635delinsA ENSP00000388058.2:p.Phe1877LeufsTer?
ENST00000524792.5:n.1846_1850delinsA
ENST00000527805.6:c.*695_*699delinsA ENSP00000435747.2:n.*695_*699delinsA
ENST00000529588.5:c.143_147delinsA
ENST00000533690.5:n.1035_1039delinsA
ENST00000675595.1:c.*695_*699delinsA ENSP00000502563.1:n.*695_*699delinsA
ENST00000683174.1:n.7115_7119delinsA
ENST00000683524.1:n.855_859delinsA
ENST00000684152.1:n.1345_1349delinsA
ENST00000713593.1:c.*5102_*5106delinsA ENSP00000518889.1:n.*5102_*5106delinsA
XM_005271561.3:c.5631_5635delinsA XP_005271618.2:p.Phe1877LeufsTer?
XM_005271562.3:c.5631_5635delinsA XP_005271619.2:p.Phe1877LeufsTer?
XM_005271562.5:c.5631_5635delinsA XP_005271619.2:p.Phe1877LeufsTer?
XM_006718843.2:c.5631_5635delinsA XP_006718906.1:p.Phe1877LeufsTer?
XM_006718843.4:c.5631_5635delinsA XP_006718906.1:p.Phe1877LeufsTer?
XM_006718845.1:c.1587_1591delinsA XP_006718908.1:p.Phe529LeufsTer?
XM_006718845.2:c.1587_1591delinsA XP_006718908.1:p.Phe529LeufsTer?
XM_011542840.1:c.5631_5635delinsA XP_011541142.1:p.Phe1877LeufsTer?
XM_011542840.3:c.5631_5635delinsA XP_011541142.1:p.Phe1877LeufsTer?
XM_011542841.1:c.5631_5635delinsA XP_011541143.1:p.Phe1877LeufsTer?
XM_011542842.1:c.5466_5470delinsA XP_011541144.1:p.Phe1822LeufsTer?
XM_011542842.3:c.5466_5470delinsA XP_011541144.1:p.Phe1822LeufsTer?
XM_011542843.1:c.5631_5635delinsA XP_011541145.1:p.Phe1877LeufsTer?
XM_011542843.2:c.5631_5635delinsA XP_011541145.1:p.Phe1877LeufsTer?
XM_011542844.1:c.4587_4591delinsA XP_011541146.1:p.Phe1529LeufsTer?
XM_011542844.3:c.4587_4591delinsA XP_011541146.1:p.Phe1529LeufsTer?
XM_011542845.1:c.4323_4327delinsA XP_011541147.1:p.Phe1441LeufsTer?
XM_011542845.2:c.4323_4327delinsA XP_011541147.1:p.Phe1441LeufsTer?
XM_011542847.1:c.702_706delinsA XP_011541149.1:p.Phe234LeufsTer?
XM_017017789.2:c.5631_5635delinsA XP_016873278.1:p.Phe1877LeufsTer?
XM_017017790.2:c.5631_5635delinsA XP_016873279.1:p.Phe1877LeufsTer?
XM_017017791.1:c.5631_5635delinsA XP_016873280.1:p.Phe1877LeufsTer?
XR_002957150.1:n.6231_6235delinsA