Canonical Allele Identifier: CA671400892
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs1356297728

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108258872_108258884del , CM000673.2:g.108258872_108258884del GRCh38
NC_000011.9:g.108129599_108129611del , CM000673.1:g.108129599_108129611del GRCh37
NC_000011.8:g.107634809_107634821del NCBI36
NG_009830.1:g.41041_41053del , LRG_135:g.41041_41053del

Transcript Alleles

HGVS Amino-acid change
ENST00000278616.8:c.2377-114_2377-102del ENSP00000278616.4:p.=
ENST00000452508.6:c.2377-114_2377-102del ENSP00000388058.2:p.=
ENST00000527805.5:c.2377-114_2377-102del ENSP00000435747.1:p.=
NM_000051.3:c.2377-114_2377-102del , LRG_135t1:c.2377-114_2377-102del NP_000042.3:p.=
XM_005271561.3:c.2377-114_2377-102del XP_005271618.2:p.=
XM_005271562.3:c.2377-114_2377-102del XP_005271619.2:p.=
XM_006718843.2:c.2377-114_2377-102del XP_006718906.1:p.=
XM_011542840.1:c.2377-114_2377-102del XP_011541142.1:p.=
XM_011542841.1:c.2377-114_2377-102del XP_011541143.1:p.=
XM_011542842.1:c.2212-114_2212-102del XP_011541144.1:p.=
XM_011542843.1:c.2377-114_2377-102del XP_011541145.1:p.=
XM_011542844.1:c.1333-114_1333-102del XP_011541146.1:p.=
XM_011542845.1:c.1069-114_1069-102del XP_011541147.1:p.=
XM_011542846.1:c.2377-114_2377-102del XP_011541148.1:p.=
NM_001351834.1:c.2377-114_2377-102del NP_001338763.1:p.=
XM_005271562.5:c.2377-114_2377-102del XP_005271619.2:p.=
XM_006718843.4:c.2377-114_2377-102del XP_006718906.1:p.=
XM_011542840.3:c.2377-114_2377-102del XP_011541142.1:p.=
XM_011542842.3:c.2212-114_2212-102del XP_011541144.1:p.=
XM_011542843.2:c.2377-114_2377-102del XP_011541145.1:p.=
XM_011542844.3:c.1333-114_1333-102del XP_011541146.1:p.=
XM_011542845.2:c.1069-114_1069-102del XP_011541147.1:p.=
XM_017017789.2:c.2377-114_2377-102del XP_016873278.1:p.=
XM_017017790.2:c.2377-114_2377-102del XP_016873279.1:p.=
XM_017017791.1:c.2377-114_2377-102del XP_016873280.1:p.=
XM_017017792.2:c.2377-114_2377-102del XP_016873281.1:p.=
NM_001351834.2:c.2377-114_2377-102del NP_001338763.1:p.=
NM_000051.4:c.2377-114_2377-102del MANE Select NP_000042.3:p.=