Canonical Allele Identifier: CA671400853

Gene: ATM

Linked Data

• dbSNP Id: rs1189400760
• MyVariant Identifiers: chr11:g.108129550_108129551del (hg19) ; chr11:g.108258823_108258824del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108258824_108258825del , CM000673.2:g.108258824_108258825del	GRCh38
NC_000011.9:g.108129551_108129552del , CM000673.1:g.108129551_108129552del	GRCh37
NC_000011.8:g.107634761_107634762del	NCBI36
NG_009830.1:g.40993_40994del , LRG_135:g.40993_40994del

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.2377-162_2377-161del	ENSP00000388058.2:n.2377-162_2377-161del
ENST00000713593.1:c.*1848-162_*1848-161del	ENSP00000518889.1:n.*1848-162_*1848-161de...
ENST00000278616.9:c.2377-162_2377-161del	ENSP00000278616.4:n.2377-162_2377-161del
ENST00000682516.1:n.2511-162_2511-161del
ENST00000683174.1:n.2527-162_2527-161del
ENST00000683605.1:n.1872-162_1872-161del
ENST00000684037.1:c.*1312-162_*1312-161del	ENSP00000508245.1:n.*1312-162_*1312-161de...
ENST00000527805.6:c.2377-162_2377-161del	ENSP00000435747.2:n.2377-162_2377-161del
ENST00000675595.1:c.2212-162_2212-161del	ENSP00000502563.1:n.2212-162_2212-161del
ENST00000675843.1:c.2377-162_2377-161del MANE Select	ENSP00000501606.1:n.2377-162_2377-161del
ENST00000278616.8:c.2377-162_2377-161del	ENSP00000278616.4:n.2377-162_2377-161del
ENST00000452508.6:c.2377-162_2377-161del	ENSP00000388058.2:n.2377-162_2377-161del
ENST00000527805.5:c.2377-162_2377-161del	ENSP00000435747.1:n.2377-162_2377-161del
NM_000051.3:c.2377-162_2377-161del , LRG_135t1:c.2377-162_2377-161del	NP_000042.3:n.2377-162_2377-161del
XM_005271561.3:c.2377-162_2377-161del	XP_005271618.2:n.2377-162_2377-161del
XM_005271562.3:c.2377-162_2377-161del	XP_005271619.2:n.2377-162_2377-161del
XM_006718843.2:c.2377-162_2377-161del	XP_006718906.1:n.2377-162_2377-161del
XM_011542840.1:c.2377-162_2377-161del	XP_011541142.1:n.2377-162_2377-161del
XM_011542841.1:c.2377-162_2377-161del	XP_011541143.1:n.2377-162_2377-161del
XM_011542842.1:c.2212-162_2212-161del	XP_011541144.1:n.2212-162_2212-161del
XM_011542843.1:c.2377-162_2377-161del	XP_011541145.1:n.2377-162_2377-161del
XM_011542844.1:c.1333-162_1333-161del	XP_011541146.1:n.1333-162_1333-161del
XM_011542845.1:c.1069-162_1069-161del	XP_011541147.1:n.1069-162_1069-161del
XM_011542846.1:c.2377-162_2377-161del	XP_011541148.1:n.2377-162_2377-161del
NM_001351834.1:c.2377-162_2377-161del	NP_001338763.1:n.2377-162_2377-161del
XM_005271562.5:c.2377-162_2377-161del	XP_005271619.2:n.2377-162_2377-161del
XM_006718843.4:c.2377-162_2377-161del	XP_006718906.1:n.2377-162_2377-161del
XM_011542840.3:c.2377-162_2377-161del	XP_011541142.1:n.2377-162_2377-161del
XM_011542842.3:c.2212-162_2212-161del	XP_011541144.1:n.2212-162_2212-161del
XM_011542843.2:c.2377-162_2377-161del	XP_011541145.1:n.2377-162_2377-161del
XM_011542844.3:c.1333-162_1333-161del	XP_011541146.1:n.1333-162_1333-161del
XM_011542845.2:c.1069-162_1069-161del	XP_011541147.1:n.1069-162_1069-161del
XM_017017789.2:c.2377-162_2377-161del	XP_016873278.1:n.2377-162_2377-161del
XM_017017790.2:c.2377-162_2377-161del	XP_016873279.1:n.2377-162_2377-161del
XM_017017791.1:c.2377-162_2377-161del	XP_016873280.1:n.2377-162_2377-161del
XM_017017792.2:c.2377-162_2377-161del	XP_016873281.1:n.2377-162_2377-161del
XR_002957150.1:n.3110-162_3110-161del
NM_001351834.2:c.2377-162_2377-161del	NP_001338763.1:n.2377-162_2377-161del
NM_000051.4:c.2377-162_2377-161del MANE Select	NP_000042.3:n.2377-162_2377-161del