Canonical Allele Identifier: CA2615844556

Gene: ATM

Linked Data

• gnomAD v4: 11-108222922-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108222922T>G , CM000673.2:g.108222922T>G	GRCh38
NC_000011.9:g.108093649T>G , CM000673.1:g.108093649T>G	GRCh37
NC_000011.8:g.107598859T>G	NCBI36
NG_009830.1:g.5091T>G , LRG_135:g.5091T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.-383T>G	ENSP00000388058.2:n.-383T>G
ENST00000683914.2:c.-295T>G	ENSP00000507649.1:n.-295T>G
ENST00000278616.8:c.-295T>G	ENSP00000278616.4:n.-295T>G
ENST00000527805.5:c.-295T>G	ENSP00000435747.1:n.-295T>G
NM_000051.3:c.-295T>G , LRG_135t1:c.-295T>G	NP_000042.3:n.-295T>G
XM_011542843.1:c.-295T>G	XP_011541145.1:n.-295T>G
XM_011542846.1:c.-295T>G	XP_011541148.1:n.-295T>G
NM_001351834.1:c.-383T>G	NP_001338763.1:n.-383T>G
NM_001351835.1:c.-295T>G	NP_001338764.1:n.-295T>G
XM_011542842.3:c.-295T>G	XP_011541144.1:n.-295T>G
XM_011542843.2:c.-295T>G	XP_011541145.1:n.-295T>G
XM_011542844.3:c.-1317T>G	XP_011541146.1:n.-1317T>G
XM_017017791.1:c.-295T>G	XP_016873280.1:n.-295T>G
XM_017017792.2:c.-295T>G	XP_016873281.1:n.-295T>G
XR_002957150.1:n.439T>G