Canonical Allele Identifier: CA2725134871

Gene: ATM

Linked Data

• dbSNP Id: rs2135510416

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108267376_108267380del , CM000673.2:g.108267376_108267380del	GRCh38
NC_000011.9:g.108138103_108138107del , CM000673.1:g.108138103_108138107del	GRCh37
NC_000011.8:g.107643313_107643317del	NCBI36
NG_009830.1:g.49545_49549del , LRG_135:g.49545_49549del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2638+34_2638+38del	ENSP00000388058.2:n.2638+34_2638+38del
ENST00000713593.1:c.*2109+34_*2109+38del	ENSP00000518889.1:n.*2109+34_*2109+38del
ENST00000278616.9:c.2638+34_2638+38del	ENSP00000278616.4:n.2638+34_2638+38del
ENST00000682516.1:n.2772+34_2772+38del
ENST00000683174.1:n.2788+34_2788+38del
ENST00000683605.1:n.2167_2171del
ENST00000684037.1:c.*1573+34_*1573+38del	ENSP00000508245.1:n.*1573+34_*1573+38del
ENST00000527805.6:c.2638+34_2638+38del	ENSP00000435747.2:n.2638+34_2638+38del
ENST00000675595.1:c.2473+34_2473+38del	ENSP00000502563.1:n.2473+34_2473+38del
ENST00000675843.1:c.2638+34_2638+38del MANE Select	ENSP00000501606.1:n.2638+34_2638+38del
ENST00000278616.8:c.2638+34_2638+38del	ENSP00000278616.4:n.2638+34_2638+38del
ENST00000452508.6:c.2638+34_2638+38del	ENSP00000388058.2:n.2638+34_2638+38del
ENST00000527805.5:c.2638+34_2638+38del	ENSP00000435747.1:n.2638+34_2638+38del
NM_000051.3:c.2638+34_2638+38del , LRG_135t1:c.2638+34_2638+38del	NP_000042.3:n.2638+34_2638+38del
XM_005271561.3:c.2638+34_2638+38del	XP_005271618.2:n.2638+34_2638+38del
XM_005271562.3:c.2638+34_2638+38del	XP_005271619.2:n.2638+34_2638+38del
XM_006718843.2:c.2638+34_2638+38del	XP_006718906.1:n.2638+34_2638+38del
XM_011542840.1:c.2638+34_2638+38del	XP_011541142.1:n.2638+34_2638+38del
XM_011542841.1:c.2638+34_2638+38del	XP_011541143.1:n.2638+34_2638+38del
XM_011542842.1:c.2473+34_2473+38del	XP_011541144.1:n.2473+34_2473+38del
XM_011542843.1:c.2638+34_2638+38del	XP_011541145.1:n.2638+34_2638+38del
XM_011542844.1:c.1594+34_1594+38del	XP_011541146.1:n.1594+34_1594+38del
XM_011542845.1:c.1330+34_1330+38del	XP_011541147.1:n.1330+34_1330+38del
XM_011542846.1:c.2638+34_2638+38del	XP_011541148.1:n.2638+34_2638+38del
NM_001351834.1:c.2638+34_2638+38del	NP_001338763.1:n.2638+34_2638+38del
XM_005271562.5:c.2638+34_2638+38del	XP_005271619.2:n.2638+34_2638+38del
XM_006718843.4:c.2638+34_2638+38del	XP_006718906.1:n.2638+34_2638+38del
XM_011542840.3:c.2638+34_2638+38del	XP_011541142.1:n.2638+34_2638+38del
XM_011542842.3:c.2473+34_2473+38del	XP_011541144.1:n.2473+34_2473+38del
XM_011542843.2:c.2638+34_2638+38del	XP_011541145.1:n.2638+34_2638+38del
XM_011542844.3:c.1594+34_1594+38del	XP_011541146.1:n.1594+34_1594+38del
XM_011542845.2:c.1330+34_1330+38del	XP_011541147.1:n.1330+34_1330+38del
XM_017017789.2:c.2638+34_2638+38del	XP_016873278.1:n.2638+34_2638+38del
XM_017017790.2:c.2638+34_2638+38del	XP_016873279.1:n.2638+34_2638+38del
XM_017017791.1:c.2638+34_2638+38del	XP_016873280.1:n.2638+34_2638+38del
XM_017017792.2:c.2638+34_2638+38del	XP_016873281.1:n.2638+34_2638+38del
XR_002957150.1:n.3371+34_3371+38del
NM_001351834.2:c.2638+34_2638+38del	NP_001338763.1:n.2638+34_2638+38del
NM_000051.4:c.2638+34_2638+38del MANE Select	NP_000042.3:n.2638+34_2638+38del