Canonical Allele Identifier: CA918952392

Gene: ATM

Linked Data

• dbSNP Id: rs1555085966

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108272716_108272717delinsAA , CM000673.2:g.108272716_108272717delinsAA	GRCh38
NC_000011.9:g.108143443_108143444delinsAA , CM000673.1:g.108143443_108143444delinsAA	GRCh37
NC_000011.8:g.107648653_107648654delinsAA	NCBI36
NG_009830.1:g.54885_54886delinsAA , LRG_135:g.54885_54886delinsAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.3154-6_3154-5delinsAA	ENSP00000388058.2:n.3154-6_3154-5delinsAA
ENST00000713593.1:c.*2625-6_*2625-5delinsAA	ENSP00000518889.1:n.*2625-6_*2625-5delinsAA
ENST00000278616.9:c.3154-6_3154-5delinsAA	ENSP00000278616.4:n.3154-6_3154-5delinsAA
ENST00000683174.1:n.3304-6_3304-5delinsAA
ENST00000527805.6:c.3154-6_3154-5delinsAA	ENSP00000435747.2:n.3154-6_3154-5delinsAA
ENST00000675595.1:c.2989-6_2989-5delinsAA	ENSP00000502563.1:n.2989-6_2989-5delinsAA
ENST00000675843.1:c.3154-6_3154-5delinsAA MANE Select	ENSP00000501606.1:n.3154-6_3154-5delinsAA
ENST00000278616.8:c.3154-6_3154-5delinsAA	ENSP00000278616.4:n.3154-6_3154-5delinsAA
ENST00000452508.6:c.3154-6_3154-5delinsAA	ENSP00000388058.2:n.3154-6_3154-5delinsAA
ENST00000527805.5:c.3154-6_3154-5delinsAA	ENSP00000435747.1:n.3154-6_3154-5delinsAA
NM_000051.3:c.3154-6_3154-5delinsAA , LRG_135t1:c.3154-6_3154-5delinsAA	NP_000042.3:n.3154-6_3154-5delinsAA
XM_005271561.3:c.3154-6_3154-5delinsAA	XP_005271618.2:n.3154-6_3154-5delinsAA
XM_005271562.3:c.3154-6_3154-5delinsAA	XP_005271619.2:n.3154-6_3154-5delinsAA
XM_006718843.2:c.3154-6_3154-5delinsAA	XP_006718906.1:n.3154-6_3154-5delinsAA
XM_011542840.1:c.3154-6_3154-5delinsAA	XP_011541142.1:n.3154-6_3154-5delinsAA
XM_011542841.1:c.3154-6_3154-5delinsAA	XP_011541143.1:n.3154-6_3154-5delinsAA
XM_011542842.1:c.2989-6_2989-5delinsAA	XP_011541144.1:n.2989-6_2989-5delinsAA
XM_011542843.1:c.3154-6_3154-5delinsAA	XP_011541145.1:n.3154-6_3154-5delinsAA
XM_011542844.1:c.2110-6_2110-5delinsAA	XP_011541146.1:n.2110-6_2110-5delinsAA
XM_011542845.1:c.1846-6_1846-5delinsAA	XP_011541147.1:n.1846-6_1846-5delinsAA
XM_011542846.1:c.3154-6_3154-5delinsAA	XP_011541148.1:n.3154-6_3154-5delinsAA
NM_001351834.1:c.3154-6_3154-5delinsAA	NP_001338763.1:n.3154-6_3154-5delinsAA
XM_005271562.5:c.3154-6_3154-5delinsAA	XP_005271619.2:n.3154-6_3154-5delinsAA
XM_006718843.4:c.3154-6_3154-5delinsAA	XP_006718906.1:n.3154-6_3154-5delinsAA
XM_011542840.3:c.3154-6_3154-5delinsAA	XP_011541142.1:n.3154-6_3154-5delinsAA
XM_011542842.3:c.2989-6_2989-5delinsAA	XP_011541144.1:n.2989-6_2989-5delinsAA
XM_011542843.2:c.3154-6_3154-5delinsAA	XP_011541145.1:n.3154-6_3154-5delinsAA
XM_011542844.3:c.2110-6_2110-5delinsAA	XP_011541146.1:n.2110-6_2110-5delinsAA
XM_011542845.2:c.1846-6_1846-5delinsAA	XP_011541147.1:n.1846-6_1846-5delinsAA
XM_017017789.2:c.3154-6_3154-5delinsAA	XP_016873278.1:n.3154-6_3154-5delinsAA
XM_017017790.2:c.3154-6_3154-5delinsAA	XP_016873279.1:n.3154-6_3154-5delinsAA
XM_017017791.1:c.3154-6_3154-5delinsAA	XP_016873280.1:n.3154-6_3154-5delinsAA
XM_017017792.2:c.3154-6_3154-5delinsAA	XP_016873281.1:n.3154-6_3154-5delinsAA
XR_002957150.1:n.3887-6_3887-5delinsAA
NM_001351834.2:c.3154-6_3154-5delinsAA	NP_001338763.1:n.3154-6_3154-5delinsAA
NM_000051.4:c.3154-6_3154-5delinsAA MANE Select	NP_000042.3:n.3154-6_3154-5delinsAA