Canonical Allele Identifier: CA476676868

Gene: ATM C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108330271G>A , CM000673.2:g.108330271G>A	GRCh38
NC_000011.9:g.108200998G>A , CM000673.1:g.108200998G>A	GRCh37
NC_000011.8:g.107706208G>A	NCBI36
NG_009830.1:g.112440G>A , LRG_135:g.112440G>A
NG_054724.1:g.144562C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000051.4:c.7365G>A (ATM) MANE Select	NP_000042.3:p.Leu2455=
ENST00000675843.1:c.7365G>A (ATM) MANE Select	ENSP00000501606.1:p.Leu2455=
NM_000051.3:c.7365G>A , LRG_135t1:c.7365G>A (ATM)	NP_000042.3:p.Leu2455=
NM_001330368.1:c.641-21200C>T (C11orf65)	NP_001317297.1:n.641-21200C>T
NM_001330368.2:c.641-21200C>T (C11orf65)	NP_001317297.1:n.641-21200C>T
NM_001351110.1:c.*38+4949C>T (C11orf65)	NP_001338039.1:n.*38+4949C>T
NM_001351110.2:c.*38+4949C>T (C11orf65)	NP_001338039.1:n.*38+4949C>T
NM_001351834.1:c.7365G>A (ATM)	NP_001338763.1:p.Leu2455=
NM_001351834.2:c.7365G>A (ATM)	NP_001338763.1:p.Leu2455=
ENST00000278616.8:c.7365G>A (ATM)	ENSP00000278616.4:p.Leu2455=
ENST00000278616.9:c.7365G>A (ATM)	ENSP00000278616.4:p.Leu2455=
ENST00000452508.6:c.7365G>A (ATM)	ENSP00000388058.2:p.Leu2455=
ENST00000452508.7:c.7365G>A (ATM)	ENSP00000388058.2:p.Leu2455=
ENST00000524792.5:n.3580G>A (ATM)
ENST00000525056.2:n.1784G>A (ATM)
ENST00000525537.3:n.322G>A (ATM)
ENST00000525729.5:c.641-21200C>T (C11orf65)	ENSP00000433395.1:n.641-21200C>T
ENST00000527805.6:c.*2429G>A (ATM)	ENSP00000435747.2:n.*2429G>A
ENST00000533690.5:n.2769G>A (ATM)
ENST00000638786.2:n.202G>A (ATM)
ENST00000675595.1:c.*2500G>A (ATM)	ENSP00000502563.1:n.*2500G>A
ENST00000682286.1:n.2122G>A (ATM)
ENST00000682302.1:n.1783G>A (ATM)
ENST00000683174.1:n.8849G>A (ATM)
ENST00000683524.1:n.2589G>A (ATM)
ENST00000684152.1:n.3079G>A (ATM)
ENST00000684447.1:n.1828G>A (ATM)
ENST00000713593.1:c.*6836G>A (ATM)	ENSP00000518889.1:n.*6836G>A
XM_005271561.3:c.7365G>A (ATM)	XP_005271618.2:p.Leu2455=
XM_005271562.3:c.7365G>A (ATM)	XP_005271619.2:p.Leu2455=
XM_005271562.5:c.7365G>A (ATM)	XP_005271619.2:p.Leu2455=
XM_006718843.2:c.7365G>A (ATM)	XP_006718906.1:p.Leu2455=
XM_006718843.4:c.7365G>A (ATM)	XP_006718906.1:p.Leu2455=
XM_006718845.1:c.3321G>A (ATM)	XP_006718908.1:p.Leu1107=
XM_006718845.2:c.3321G>A (ATM)	XP_006718908.1:p.Leu1107=
XM_011542840.1:c.7365G>A (ATM)	XP_011541142.1:p.Leu2455=
XM_011542840.3:c.7365G>A (ATM)	XP_011541142.1:p.Leu2455=
XM_011542841.1:c.7365G>A (ATM)	XP_011541143.1:p.Leu2455=
XM_011542842.1:c.7200G>A (ATM)	XP_011541144.1:p.Leu2400=
XM_011542842.3:c.7200G>A (ATM)	XP_011541144.1:p.Leu2400=
XM_011542843.1:c.7365G>A (ATM)	XP_011541145.1:p.Leu2455=
XM_011542843.2:c.7365G>A (ATM)	XP_011541145.1:p.Leu2455=
XM_011542844.1:c.6321G>A (ATM)	XP_011541146.1:p.Leu2107=
XM_011542844.3:c.6321G>A (ATM)	XP_011541146.1:p.Leu2107=
XM_011542845.1:c.6057G>A (ATM)	XP_011541147.1:p.Leu2019=
XM_011542845.2:c.6057G>A (ATM)	XP_011541147.1:p.Leu2019=
XM_011542847.1:c.2436G>A (ATM)	XP_011541149.1:p.Leu812=
XM_017017789.2:c.7365G>A (ATM)	XP_016873278.1:p.Leu2455=
XM_017017790.2:c.7365G>A (ATM)	XP_016873279.1:p.Leu2455=