Canonical Allele Identifier: CA382525836

Gene: ATM

Linked Data

• MyVariant Identifiers: chr11:g.108106566G>T (hg19) ; chr11:g.108235839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108235839G>T , CM000673.2:g.108235839G>T	GRCh38
NC_000011.9:g.108106566G>T , CM000673.1:g.108106566G>T	GRCh37
NC_000011.8:g.107611776G>T	NCBI36
NG_009830.1:g.18008G>T , LRG_135:g.18008G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.496+5G>T	ENSP00000388058.2:n.496+5G>T
ENST00000713593.1:c.496+5G>T	ENSP00000518889.1:n.496+5G>T
ENST00000278616.9:c.496+5G>T	ENSP00000278616.4:n.496+5G>T
ENST00000682147.1:n.631G>T
ENST00000682430.1:n.595+5G>T
ENST00000682516.1:n.630+5G>T
ENST00000682956.1:n.630+5G>T
ENST00000683174.1:n.646+5G>T
ENST00000684029.1:c.501G>T	ENSP00000508010.1:p.Met167Ile
ENST00000684037.1:c.496+5G>T	ENSP00000508245.1:n.496+5G>T
ENST00000684061.1:n.630+5G>T
ENST00000684179.1:n.465+6516G>T
ENST00000527805.6:c.496+5G>T	ENSP00000435747.2:n.496+5G>T
ENST00000675595.1:c.331+6516G>T	ENSP00000502563.1:n.331+6516G>T
ENST00000675843.1:c.496+5G>T MANE Select	ENSP00000501606.1:n.496+5G>T
ENST00000278616.8:c.496+5G>T	ENSP00000278616.4:n.496+5G>T
ENST00000452508.6:c.496+5G>T	ENSP00000388058.2:n.496+5G>T
ENST00000527805.5:c.496+5G>T	ENSP00000435747.1:n.496+5G>T
ENST00000527891.5:c.331+6516G>T	ENSP00000433955.1:n.331+6516G>T
ENST00000530958.5:c.501G>T	ENSP00000483338.1:p.Met167Ile
NM_000051.3:c.496+5G>T , LRG_135t1:c.496+5G>T	NP_000042.3:n.496+5G>T
XM_005271561.3:c.496+5G>T	XP_005271618.2:n.496+5G>T
XM_005271562.3:c.496+5G>T	XP_005271619.2:n.496+5G>T
XM_006718843.2:c.496+5G>T	XP_006718906.1:n.496+5G>T
XM_011542840.1:c.496+5G>T	XP_011541142.1:n.496+5G>T
XM_011542841.1:c.496+5G>T	XP_011541143.1:n.496+5G>T
XM_011542842.1:c.331+6516G>T	XP_011541144.1:n.331+6516G>T
XM_011542843.1:c.496+5G>T	XP_011541145.1:n.496+5G>T
XM_011542844.1:c.-527+5G>T	XP_011541146.1:n.-527+5G>T
XM_011542846.1:c.496+5G>T	XP_011541148.1:n.496+5G>T
NM_001351834.1:c.496+5G>T	NP_001338763.1:n.496+5G>T
XM_005271562.5:c.496+5G>T	XP_005271619.2:n.496+5G>T
XM_006718843.4:c.496+5G>T	XP_006718906.1:n.496+5G>T
XM_011542840.3:c.496+5G>T	XP_011541142.1:n.496+5G>T
XM_011542842.3:c.331+6516G>T	XP_011541144.1:n.331+6516G>T
XM_011542843.2:c.496+5G>T	XP_011541145.1:n.496+5G>T
XM_011542844.3:c.-527+5G>T	XP_011541146.1:n.-527+5G>T
XM_017017789.2:c.496+5G>T	XP_016873278.1:n.496+5G>T
XM_017017790.2:c.496+5G>T	XP_016873279.1:n.496+5G>T
XM_017017791.1:c.496+5G>T	XP_016873280.1:n.496+5G>T
XM_017017792.2:c.496+5G>T	XP_016873281.1:n.496+5G>T
XR_002957150.1:n.1229+5G>T
NM_001351834.2:c.496+5G>T	NP_001338763.1:n.496+5G>T
NM_000051.4:c.496+5G>T MANE Select	NP_000042.3:n.496+5G>T