Canonical Allele Identifier: CA2695215354

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108244090_108244096del , CM000673.2:g.108244090_108244096del	GRCh38
NC_000011.9:g.108114817_108114823del , CM000673.1:g.108114817_108114823del	GRCh37
NC_000011.8:g.107620027_107620033del	NCBI36
NG_009830.1:g.26259_26265del , LRG_135:g.26259_26265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.634_640del	ENSP00000388058.2:p.Phe212ProfsTer16
ENST00000713593.1:c.*105_*111del	ENSP00000518889.1:n.*105_*111del
ENST00000278616.9:c.634_640del	ENSP00000278616.4:p.Phe212ProfsTer16
ENST00000682430.1:n.733_739del
ENST00000682516.1:n.768_774del
ENST00000682956.1:n.768_774del
ENST00000683100.1:n.2312_2318del
ENST00000683174.1:n.784_790del
ENST00000683605.1:n.129_135del
ENST00000684037.1:c.634_640del	ENSP00000508245.1:p.Phe212ProfsTer16
ENST00000684061.1:n.768_774del
ENST00000684179.1:n.603_609del
ENST00000527805.6:c.634_640del	ENSP00000435747.2:p.Phe212ProfsTer16
ENST00000675595.1:c.469_475del	ENSP00000502563.1:p.Phe157ProfsTer16
ENST00000675843.1:c.634_640del MANE Select	ENSP00000501606.1:p.Phe212ProfsTer16
ENST00000278616.8:c.634_640del	ENSP00000278616.4:p.Phe212ProfsTer16
ENST00000452508.6:c.634_640del	ENSP00000388058.2:p.Phe212ProfsTer16
ENST00000527805.5:c.634_640del	ENSP00000435747.1:p.Phe212ProfsTer16
NM_000051.3:c.634_640del , LRG_135t1:c.634_640del	NP_000042.3:p.Phe212ProfsTer16
XM_005271561.3:c.634_640del	XP_005271618.2:p.Phe212ProfsTer16
XM_005271562.3:c.634_640del	XP_005271619.2:p.Phe212ProfsTer16
XM_006718843.2:c.634_640del	XP_006718906.1:p.Phe212ProfsTer16
XM_011542840.1:c.634_640del	XP_011541142.1:p.Phe212ProfsTer16
XM_011542841.1:c.634_640del	XP_011541143.1:p.Phe212ProfsTer16
XM_011542842.1:c.469_475del	XP_011541144.1:p.Phe157ProfsTer16
XM_011542843.1:c.634_640del	XP_011541145.1:p.Phe212ProfsTer16
XM_011542844.1:c.-411_-405del	XP_011541146.1:n.-411_-405del
XM_011542846.1:c.634_640del	XP_011541148.1:p.Phe212ProfsTer16
NM_001351834.1:c.634_640del	NP_001338763.1:p.Phe212ProfsTer16
XM_005271562.5:c.634_640del	XP_005271619.2:p.Phe212ProfsTer16
XM_006718843.4:c.634_640del	XP_006718906.1:p.Phe212ProfsTer16
XM_011542840.3:c.634_640del	XP_011541142.1:p.Phe212ProfsTer16
XM_011542842.3:c.469_475del	XP_011541144.1:p.Phe157ProfsTer16
XM_011542843.2:c.634_640del	XP_011541145.1:p.Phe212ProfsTer16
XM_011542844.3:c.-411_-405del	XP_011541146.1:n.-411_-405del
XM_017017789.2:c.634_640del	XP_016873278.1:p.Phe212ProfsTer16
XM_017017790.2:c.634_640del	XP_016873279.1:p.Phe212ProfsTer16
XM_017017791.1:c.634_640del	XP_016873280.1:p.Phe212ProfsTer16
XM_017017792.2:c.634_640del	XP_016873281.1:p.Phe212ProfsTer16
XR_002957150.1:n.1367_1373del
NM_001351834.2:c.634_640del	NP_001338763.1:p.Phe212ProfsTer16
NM_000051.4:c.634_640del MANE Select	NP_000042.3:p.Phe212ProfsTer16