Canonical Allele Identifier: CA645569737

Gene: ATM

Linked Data

• COSMIC: COSM6444446 ; COSM6444447

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253939_108253957del , CM000673.2:g.108253939_108253957del	GRCh38
NC_000011.9:g.108124666_108124684del , CM000673.1:g.108124666_108124684del	GRCh37
NC_000011.8:g.107629876_107629894del	NCBI36
NG_009830.1:g.36108_36126del , LRG_135:g.36108_36126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2024_2042del	ENSP00000388058.2:p.Gln675LeufsTer22
ENST00000713593.1:c.*1495_*1513del	ENSP00000518889.1:n.*1495_*1513del
ENST00000278616.9:c.2024_2042del	ENSP00000278616.4:p.Gln675LeufsTer22
ENST00000682516.1:n.2158_2176del
ENST00000683174.1:n.2174_2192del
ENST00000683605.1:n.1519_1537del
ENST00000684037.1:c.*959_*977del	ENSP00000508245.1:n.*959_*977del
ENST00000684061.1:n.2158_2176del
ENST00000527805.6:c.2024_2042del	ENSP00000435747.2:p.Gln675LeufsTer22
ENST00000675595.1:c.1859_1877del	ENSP00000502563.1:p.Gln620LeufsTer22
ENST00000675843.1:c.2024_2042del MANE Select	ENSP00000501606.1:p.Gln675LeufsTer22
ENST00000278616.8:c.2024_2042del	ENSP00000278616.4:p.Gln675LeufsTer22
ENST00000452508.6:c.2024_2042del	ENSP00000388058.2:p.Gln675LeufsTer22
ENST00000525012.5:n.201_219del
ENST00000527805.5:c.2024_2042del	ENSP00000435747.1:p.Gln675LeufsTer22
ENST00000533526.1:n.177_195del
NM_000051.3:c.2024_2042del , LRG_135t1:c.2024_2042del	NP_000042.3:p.Gln675LeufsTer22
XM_005271561.3:c.2024_2042del	XP_005271618.2:p.Gln675LeufsTer22
XM_005271562.3:c.2024_2042del	XP_005271619.2:p.Gln675LeufsTer22
XM_006718843.2:c.2024_2042del	XP_006718906.1:p.Gln675LeufsTer22
XM_011542840.1:c.2024_2042del	XP_011541142.1:p.Gln675LeufsTer22
XM_011542841.1:c.2024_2042del	XP_011541143.1:p.Gln675LeufsTer22
XM_011542842.1:c.1859_1877del	XP_011541144.1:p.Gln620LeufsTer22
XM_011542843.1:c.2024_2042del	XP_011541145.1:p.Gln675LeufsTer22
XM_011542844.1:c.980_998del	XP_011541146.1:p.Gln327LeufsTer22
XM_011542845.1:c.716_734del	XP_011541147.1:p.Gln239LeufsTer22
XM_011542846.1:c.2024_2042del	XP_011541148.1:p.Gln675LeufsTer22
NM_001351834.1:c.2024_2042del	NP_001338763.1:p.Gln675LeufsTer22
XM_005271562.5:c.2024_2042del	XP_005271619.2:p.Gln675LeufsTer22
XM_006718843.4:c.2024_2042del	XP_006718906.1:p.Gln675LeufsTer22
XM_011542840.3:c.2024_2042del	XP_011541142.1:p.Gln675LeufsTer22
XM_011542842.3:c.1859_1877del	XP_011541144.1:p.Gln620LeufsTer22
XM_011542843.2:c.2024_2042del	XP_011541145.1:p.Gln675LeufsTer22
XM_011542844.3:c.980_998del	XP_011541146.1:p.Gln327LeufsTer22
XM_011542845.2:c.716_734del	XP_011541147.1:p.Gln239LeufsTer22
XM_017017789.2:c.2024_2042del	XP_016873278.1:p.Gln675LeufsTer22
XM_017017790.2:c.2024_2042del	XP_016873279.1:p.Gln675LeufsTer22
XM_017017791.1:c.2024_2042del	XP_016873280.1:p.Gln675LeufsTer22
XM_017017792.2:c.2024_2042del	XP_016873281.1:p.Gln675LeufsTer22
XR_002957150.1:n.2757_2775del
NM_001351834.2:c.2024_2042del	NP_001338763.1:p.Gln675LeufsTer22
NM_000051.4:c.2024_2042del MANE Select	NP_000042.3:p.Gln675LeufsTer22