Canonical Allele Identifier: CA382531408

Gene: ATM

Linked Data

• ClinVar Variation Id: 485229
• ClinVar RCV Id: RCV000570204 ; RCV003767218
• dbSNP Id: rs1555068492
• MyVariant Identifiers: chr11:g.108117797T>G (hg19) ; chr11:g.108247070T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108247070T>G , CM000673.2:g.108247070T>G	GRCh38
NC_000011.9:g.108117797T>G , CM000673.1:g.108117797T>G	GRCh37
NC_000011.8:g.107623007T>G	NCBI36
NG_009830.1:g.29239T>G , LRG_135:g.29239T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1008T>G	ENSP00000388058.2:p.Phe336Leu
ENST00000713593.1:c.*479T>G	ENSP00000518889.1:n.*479T>G
ENST00000278616.9:c.1008T>G	ENSP00000278616.4:p.Phe336Leu
ENST00000682516.1:n.1142T>G
ENST00000682956.1:n.1142T>G
ENST00000683100.1:n.3355T>G
ENST00000683174.1:n.1158T>G
ENST00000683605.1:n.503T>G
ENST00000684037.1:c.1008T>G	ENSP00000508245.1:p.Phe336Leu
ENST00000684061.1:n.1142T>G
ENST00000684179.1:n.977T>G
ENST00000527805.6:c.1008T>G	ENSP00000435747.2:p.Phe336Leu
ENST00000675595.1:c.843T>G	ENSP00000502563.1:p.Phe281Leu
ENST00000675843.1:c.1008T>G MANE Select	ENSP00000501606.1:p.Phe336Leu
ENST00000278616.8:c.1008T>G	ENSP00000278616.4:p.Phe336Leu
ENST00000452508.6:c.1008T>G	ENSP00000388058.2:p.Phe336Leu
ENST00000527805.5:c.1008T>G	ENSP00000435747.1:p.Phe336Leu
NM_000051.3:c.1008T>G , LRG_135t1:c.1008T>G	NP_000042.3:p.Phe336Leu
XM_005271561.3:c.1008T>G	XP_005271618.2:p.Phe336Leu
XM_005271562.3:c.1008T>G	XP_005271619.2:p.Phe336Leu
XM_006718843.2:c.1008T>G	XP_006718906.1:p.Phe336Leu
XM_011542840.1:c.1008T>G	XP_011541142.1:p.Phe336Leu
XM_011542841.1:c.1008T>G	XP_011541143.1:p.Phe336Leu
XM_011542842.1:c.843T>G	XP_011541144.1:p.Phe281Leu
XM_011542843.1:c.1008T>G	XP_011541145.1:p.Phe336Leu
XM_011542844.1:c.-37T>G	XP_011541146.1:n.-37T>G
XM_011542845.1:c.-131T>G	XP_011541147.1:n.-131T>G
XM_011542846.1:c.1008T>G	XP_011541148.1:p.Phe336Leu
NM_001351834.1:c.1008T>G	NP_001338763.1:p.Phe336Leu
XM_005271562.5:c.1008T>G	XP_005271619.2:p.Phe336Leu
XM_006718843.4:c.1008T>G	XP_006718906.1:p.Phe336Leu
XM_011542840.3:c.1008T>G	XP_011541142.1:p.Phe336Leu
XM_011542842.3:c.843T>G	XP_011541144.1:p.Phe281Leu
XM_011542843.2:c.1008T>G	XP_011541145.1:p.Phe336Leu
XM_011542844.3:c.-37T>G	XP_011541146.1:n.-37T>G
XM_011542845.2:c.-131T>G	XP_011541147.1:n.-131T>G
XM_017017789.2:c.1008T>G	XP_016873278.1:p.Phe336Leu
XM_017017790.2:c.1008T>G	XP_016873279.1:p.Phe336Leu
XM_017017791.1:c.1008T>G	XP_016873280.1:p.Phe336Leu
XM_017017792.2:c.1008T>G	XP_016873281.1:p.Phe336Leu
XR_002957150.1:n.1741T>G
NM_001351834.2:c.1008T>G	NP_001338763.1:p.Phe336Leu
NM_000051.4:c.1008T>G MANE Select	NP_000042.3:p.Phe336Leu