Canonical Allele Identifier: CA10579143

Gene: ATM

Linked Data

• ClinVar Variation Id: 232436
• ClinVar RCV Id: RCV000220936 ; RCV000797213 ; RCV003462497
• dbSNP Id: rs876659764
• gnomAD v4: 11-108289630-T-C
• MyVariant Identifiers: chr11:g.108160357T>C (hg19) ; chr11:g.108289630T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108289630T>C , CM000673.2:g.108289630T>C	GRCh38
NC_000011.9:g.108160357T>C , CM000673.1:g.108160357T>C	GRCh37
NC_000011.8:g.107665567T>C	NCBI36
NG_009830.1:g.71799T>C , LRG_135:g.71799T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.4265T>C	ENSP00000388058.2:p.Ile1422Thr
ENST00000713593.1:c.*3736T>C	ENSP00000518889.1:n.*3736T>C
ENST00000278616.9:c.4265T>C	ENSP00000278616.4:p.Ile1422Thr
ENST00000533733.6:n.1528T>C
ENST00000683174.1:n.4415T>C
ENST00000527805.6:c.4265T>C	ENSP00000435747.2:p.Ile1422Thr
ENST00000675595.1:c.4100T>C	ENSP00000502563.1:p.Ile1367Thr
ENST00000675843.1:c.4265T>C MANE Select	ENSP00000501606.1:p.Ile1422Thr
ENST00000278616.8:c.4265T>C	ENSP00000278616.4:p.Ile1422Thr
ENST00000452508.6:c.4265T>C	ENSP00000388058.2:p.Ile1422Thr
ENST00000524792.5:n.480T>C
ENST00000531525.2:c.272T>C	ENSP00000434327.2:p.Ile91Thr
ENST00000533733.5:n.694T>C
NM_000051.3:c.4265T>C , LRG_135t1:c.4265T>C	NP_000042.3:p.Ile1422Thr
XM_005271561.3:c.4265T>C	XP_005271618.2:p.Ile1422Thr
XM_005271562.3:c.4265T>C	XP_005271619.2:p.Ile1422Thr
XM_006718843.2:c.4265T>C	XP_006718906.1:p.Ile1422Thr
XM_006718845.1:c.221T>C	XP_006718908.1:p.Ile74Thr
XM_011542840.1:c.4265T>C	XP_011541142.1:p.Ile1422Thr
XM_011542841.1:c.4265T>C	XP_011541143.1:p.Ile1422Thr
XM_011542842.1:c.4100T>C	XP_011541144.1:p.Ile1367Thr
XM_011542843.1:c.4265T>C	XP_011541145.1:p.Ile1422Thr
XM_011542844.1:c.3221T>C	XP_011541146.1:p.Ile1074Thr
XM_011542845.1:c.2957T>C	XP_011541147.1:p.Ile986Thr
XM_011542846.1:c.4265T>C	XP_011541148.1:p.Ile1422Thr
NM_001351834.1:c.4265T>C	NP_001338763.1:p.Ile1422Thr
XM_005271562.5:c.4265T>C	XP_005271619.2:p.Ile1422Thr
XM_006718843.4:c.4265T>C	XP_006718906.1:p.Ile1422Thr
XM_006718845.2:c.221T>C	XP_006718908.1:p.Ile74Thr
XM_011542840.3:c.4265T>C	XP_011541142.1:p.Ile1422Thr
XM_011542842.3:c.4100T>C	XP_011541144.1:p.Ile1367Thr
XM_011542843.2:c.4265T>C	XP_011541145.1:p.Ile1422Thr
XM_011542844.3:c.3221T>C	XP_011541146.1:p.Ile1074Thr
XM_011542845.2:c.2957T>C	XP_011541147.1:p.Ile986Thr
XM_017017789.2:c.4265T>C	XP_016873278.1:p.Ile1422Thr
XM_017017790.2:c.4265T>C	XP_016873279.1:p.Ile1422Thr
XM_017017791.1:c.4265T>C	XP_016873280.1:p.Ile1422Thr
XM_017017792.2:c.4265T>C	XP_016873281.1:p.Ile1422Thr
XR_002957150.1:n.4998T>C
NM_001351834.2:c.4265T>C	NP_001338763.1:p.Ile1422Thr
NM_000051.4:c.4265T>C MANE Select	NP_000042.3:p.Ile1422Thr