Canonical Allele Identifier: CA2615844516
Gene: ATM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108222907_108222908insGGCTCGCCCT , CM000673.2:g.108222907_108222908insGGCTCGCCCT GRCh38
NC_000011.9:g.108093634_108093635insGGCTCGCCCT , CM000673.1:g.108093634_108093635insGGCTCGCCCT GRCh37
NC_000011.8:g.107598844_107598845insGGCTCGCCCT NCBI36
NG_009830.1:g.5076_5077insGGCTCGCCCT , LRG_135:g.5076_5077insGGCTCGCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-398_-397insGGCTCGCCCT ENSP00000388058.2:n.-398_-397insGGCTCGCCCT
ENST00000683914.2:c.-310_-309insGGCTCGCCCT ENSP00000507649.1:n.-310_-309insGGCTCGCCCT
ENST00000278616.8:c.-310_-309insGGCTCGCCCT ENSP00000278616.4:n.-310_-309insGGCTCGCCCT
ENST00000527805.5:c.-310_-309insGGCTCGCCCT ENSP00000435747.1:n.-310_-309insGGCTCGCCCT
NM_000051.3:c.-310_-309insGGCTCGCCCT , LRG_135t1:c.-310_-309insGGCTCGCCCT NP_000042.3:n.-310_-309insGGCTCGCCCT
XM_011542843.1:c.-310_-309insGGCTCGCCCT XP_011541145.1:n.-310_-309insGGCTCGCCCT
XM_011542846.1:c.-310_-309insGGCTCGCCCT XP_011541148.1:n.-310_-309insGGCTCGCCCT
NM_001351834.1:c.-398_-397insGGCTCGCCCT NP_001338763.1:n.-398_-397insGGCTCGCCCT
NM_001351835.1:c.-310_-309insGGCTCGCCCT NP_001338764.1:n.-310_-309insGGCTCGCCCT
XM_011542842.3:c.-310_-309insGGCTCGCCCT XP_011541144.1:n.-310_-309insGGCTCGCCCT
XM_011542843.2:c.-310_-309insGGCTCGCCCT XP_011541145.1:n.-310_-309insGGCTCGCCCT
XM_011542844.3:c.-1332_-1331insGGCTCGCCCT XP_011541146.1:n.-1332_-1331insGGCTCGCCCT
XM_017017791.1:c.-310_-309insGGCTCGCCCT XP_016873280.1:n.-310_-309insGGCTCGCCCT
XM_017017792.2:c.-310_-309insGGCTCGCCCT XP_016873281.1:n.-310_-309insGGCTCGCCCT
XR_002957150.1:n.424_425insGGCTCGCCCT