Canonical Allele Identifier: CA382559142

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327745C>A , CM000673.2:g.108327745C>A	GRCh38
NC_000011.9:g.108198472C>A , CM000673.1:g.108198472C>A	GRCh37
NC_000011.8:g.107703682C>A	NCBI36
NG_009830.1:g.109914C>A , LRG_135:g.109914C>A
NG_054724.1:g.147088G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000051.4:c.7076C>A (ATM) MANE Select	NP_000042.3:p.Thr2359Asn
ENST00000675843.1:c.7076C>A (ATM) MANE Select	ENSP00000501606.1:p.Thr2359Asn
NM_000051.3:c.7076C>A , LRG_135t1:c.7076C>A (ATM)	NP_000042.3:p.Thr2359Asn
NM_001330368.1:c.641-18674G>T (C11orf65)	NP_001317297.1:n.641-18674G>T
NM_001330368.2:c.641-18674G>T (C11orf65)	NP_001317297.1:n.641-18674G>T
NM_001351110.1:c.*38+7475G>T (C11orf65)	NP_001338039.1:n.*38+7475G>T
NM_001351110.2:c.*38+7475G>T (C11orf65)	NP_001338039.1:n.*38+7475G>T
NM_001351834.1:c.7076C>A (ATM)	NP_001338763.1:p.Thr2359Asn
NM_001351834.2:c.7076C>A (ATM)	NP_001338763.1:p.Thr2359Asn
ENST00000278616.8:c.7076C>A (ATM)	ENSP00000278616.4:p.Thr2359Asn
ENST00000278616.9:c.7076C>A (ATM)	ENSP00000278616.4:p.Thr2359Asn
ENST00000452508.6:c.7076C>A (ATM)	ENSP00000388058.2:p.Thr2359Asn
ENST00000452508.7:c.7076C>A (ATM)	ENSP00000388058.2:p.Thr2359Asn
ENST00000524792.5:n.3291C>A (ATM)
ENST00000525056.2:n.1495C>A (ATM)
ENST00000525537.2:n.352C>A (ATM)
ENST00000525537.3:n.33C>A (ATM)
ENST00000525729.5:c.641-18674G>T (C11orf65)	ENSP00000433395.1:n.641-18674G>T
ENST00000527389.2:n.101C>A (ATM)
ENST00000527805.6:c.*2140C>A (ATM)	ENSP00000435747.2:n.*2140C>A
ENST00000533690.5:n.2480C>A (ATM)
ENST00000675595.1:c.*2211C>A (ATM)	ENSP00000502563.1:n.*2211C>A
ENST00000682286.1:n.1833C>A (ATM)
ENST00000682302.1:n.1494C>A (ATM)
ENST00000683174.1:n.8560C>A (ATM)
ENST00000683524.1:n.2300C>A (ATM)
ENST00000684152.1:n.2790C>A (ATM)
ENST00000684447.1:n.1539C>A (ATM)
ENST00000713593.1:c.*6547C>A (ATM)	ENSP00000518889.1:n.*6547C>A
XM_005271561.3:c.7076C>A (ATM)	XP_005271618.2:p.Thr2359Asn
XM_005271562.3:c.7076C>A (ATM)	XP_005271619.2:p.Thr2359Asn
XM_005271562.5:c.7076C>A (ATM)	XP_005271619.2:p.Thr2359Asn
XM_006718843.2:c.7076C>A (ATM)	XP_006718906.1:p.Thr2359Asn
XM_006718843.4:c.7076C>A (ATM)	XP_006718906.1:p.Thr2359Asn
XM_006718845.1:c.3032C>A (ATM)	XP_006718908.1:p.Thr1011Asn
XM_006718845.2:c.3032C>A (ATM)	XP_006718908.1:p.Thr1011Asn
XM_011542840.1:c.7076C>A (ATM)	XP_011541142.1:p.Thr2359Asn
XM_011542840.3:c.7076C>A (ATM)	XP_011541142.1:p.Thr2359Asn
XM_011542841.1:c.7076C>A (ATM)	XP_011541143.1:p.Thr2359Asn
XM_011542842.1:c.6911C>A (ATM)	XP_011541144.1:p.Thr2304Asn
XM_011542842.3:c.6911C>A (ATM)	XP_011541144.1:p.Thr2304Asn
XM_011542843.1:c.7076C>A (ATM)	XP_011541145.1:p.Thr2359Asn
XM_011542843.2:c.7076C>A (ATM)	XP_011541145.1:p.Thr2359Asn
XM_011542844.1:c.6032C>A (ATM)	XP_011541146.1:p.Thr2011Asn
XM_011542844.3:c.6032C>A (ATM)	XP_011541146.1:p.Thr2011Asn
XM_011542845.1:c.5768C>A (ATM)	XP_011541147.1:p.Thr1923Asn
XM_011542845.2:c.5768C>A (ATM)	XP_011541147.1:p.Thr1923Asn
XM_011542847.1:c.2147C>A (ATM)	XP_011541149.1:p.Thr716Asn
XM_017017789.2:c.7076C>A (ATM)	XP_016873278.1:p.Thr2359Asn
XM_017017790.2:c.7076C>A (ATM)	XP_016873279.1:p.Thr2359Asn