Canonical Allele Identifier: CA2725185520

Gene: ATM

Linked Data

• dbSNP Id: rs2135974013

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307850G>C , CM000673.2:g.108307850G>C	GRCh38
NC_000011.9:g.108178577G>C , CM000673.1:g.108178577G>C	GRCh37
NC_000011.8:g.107683787G>C	NCBI36
NG_009830.1:g.90019G>C , LRG_135:g.90019G>C
NG_054724.1:g.166983C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.5675-47G>C	ENSP00000388058.2:n.5675-47G>C
ENST00000713593.1:c.*5146-47G>C	ENSP00000518889.1:n.*5146-47G>C
ENST00000278616.9:c.5675-47G>C	ENSP00000278616.4:n.5675-47G>C
ENST00000525056.2:n.47G>C
ENST00000682286.1:n.432-47G>C
ENST00000682302.1:n.46G>C
ENST00000683174.1:n.7159-47G>C
ENST00000683524.1:n.899-47G>C
ENST00000684152.1:n.1389-47G>C
ENST00000527805.6:c.*739-47G>C	ENSP00000435747.2:n.*739-47G>C
ENST00000675595.1:c.*739-47G>C	ENSP00000502563.1:n.*739-47G>C
ENST00000675843.1:c.5675-47G>C MANE Select	ENSP00000501606.1:n.5675-47G>C
ENST00000278616.8:c.5675-47G>C	ENSP00000278616.4:n.5675-47G>C
ENST00000452508.6:c.5675-47G>C	ENSP00000388058.2:n.5675-47G>C
ENST00000524792.5:n.1890-47G>C
ENST00000529588.5:c.187-2310G>C
ENST00000533690.5:n.1079-47G>C
NM_000051.3:c.5675-47G>C , LRG_135t1:c.5675-47G>C	NP_000042.3:n.5675-47G>C
XM_005271561.3:c.5675-47G>C	XP_005271618.2:n.5675-47G>C
XM_005271562.3:c.5675-47G>C	XP_005271619.2:n.5675-47G>C
XM_006718843.2:c.5675-47G>C	XP_006718906.1:n.5675-47G>C
XM_006718845.1:c.1631-47G>C	XP_006718908.1:n.1631-47G>C
XM_011542840.1:c.5675-47G>C	XP_011541142.1:n.5675-47G>C
XM_011542841.1:c.5675-47G>C	XP_011541143.1:n.5675-47G>C
XM_011542842.1:c.5510-47G>C	XP_011541144.1:n.5510-47G>C
XM_011542843.1:c.5675-47G>C	XP_011541145.1:n.5675-47G>C
XM_011542844.1:c.4631-47G>C	XP_011541146.1:n.4631-47G>C
XM_011542845.1:c.4367-47G>C	XP_011541147.1:n.4367-47G>C
XM_011542847.1:c.746-47G>C	XP_011541149.1:n.746-47G>C
NM_001351834.1:c.5675-47G>C	NP_001338763.1:n.5675-47G>C
XM_005271562.5:c.5675-47G>C	XP_005271619.2:n.5675-47G>C
XM_006718843.4:c.5675-47G>C	XP_006718906.1:n.5675-47G>C
XM_006718845.2:c.1631-47G>C	XP_006718908.1:n.1631-47G>C
XM_011542840.3:c.5675-47G>C	XP_011541142.1:n.5675-47G>C
XM_011542842.3:c.5510-47G>C	XP_011541144.1:n.5510-47G>C
XM_011542843.2:c.5675-47G>C	XP_011541145.1:n.5675-47G>C
XM_011542844.3:c.4631-47G>C	XP_011541146.1:n.4631-47G>C
XM_011542845.2:c.4367-47G>C	XP_011541147.1:n.4367-47G>C
XM_017017789.2:c.5675-47G>C	XP_016873278.1:n.5675-47G>C
XM_017017790.2:c.5675-47G>C	XP_016873279.1:n.5675-47G>C
XM_017017791.1:c.5675-47G>C	XP_016873280.1:n.5675-47G>C
XR_002957150.1:n.6275-47G>C
NM_001351834.2:c.5675-47G>C	NP_001338763.1:n.5675-47G>C
NM_000051.4:c.5675-47G>C MANE Select	NP_000042.3:n.5675-47G>C