Canonical Allele Identifier: CA2695215398
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108307897_108307984del , CM000673.2:g.108307897_108307984del GRCh38
NC_000011.9:g.108178624_108178711del , CM000673.1:g.108178624_108178711del GRCh37
NC_000011.8:g.107683834_107683921del NCBI36
NG_009830.1:g.90066_90153del , LRG_135:g.90066_90153del
NG_054724.1:g.166851_166938del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.5675_5762del
ENST00000713593.1:c.*5146_*5233del
ENST00000278616.9:c.5675_5762del
ENST00000525056.2:n.94_181del
ENST00000682286.1:n.432_519del
ENST00000682302.1:n.93_180del
ENST00000683174.1:n.7159_7246del
ENST00000683524.1:n.899_986del
ENST00000684152.1:n.1389_1476del
ENST00000527805.6:c.*739_*826del
ENST00000675595.1:c.*739_*826del
ENST00000675843.1:c.5675_5762del
ENST00000278616.8:c.5675_5762del
ENST00000452508.6:c.5675_5762del
ENST00000524792.5:n.1890_1977del
ENST00000529588.5:c.187-2263_187-2176del
ENST00000533690.5:n.1079_1166del
NM_000051.3:c.5675_5762del , LRG_135t1:c.5675_5762del
XM_005271561.3:c.5675_5762del
XM_005271562.3:c.5675_5762del
XM_006718843.2:c.5675_5762del
XM_006718845.1:c.1631_1718del
XM_011542840.1:c.5675_5762del
XM_011542841.1:c.5675_5762del
XM_011542842.1:c.5510_5597del
XM_011542843.1:c.5675_5762del
XM_011542844.1:c.4631_4718del
XM_011542845.1:c.4367_4454del
XM_011542847.1:c.746_833del
NM_001351834.1:c.5675_5762del
XM_005271562.5:c.5675_5762del
XM_006718843.4:c.5675_5762del
XM_006718845.2:c.1631_1718del
XM_011542840.3:c.5675_5762del
XM_011542842.3:c.5510_5597del
XM_011542843.2:c.5675_5762del
XM_011542844.3:c.4631_4718del
XM_011542845.2:c.4367_4454del
XM_017017789.2:c.5675_5762del
XM_017017790.2:c.5675_5762del
XM_017017791.1:c.5675_5762del
XR_002957150.1:n.6275_6362del
NM_001351834.2:c.5675_5762del
NM_000051.4:c.5675_5762del