Canonical Allele Identifier: CA382560071
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758673
ClinVar RCV Id: RCV002380469

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108330299A>G , CM000673.2:g.108330299A>G GRCh38
NC_000011.9:g.108201026A>G , CM000673.1:g.108201026A>G GRCh37
NC_000011.8:g.107706236A>G NCBI36
NG_009830.1:g.112468A>G , LRG_135:g.112468A>G
NG_054724.1:g.144534T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.7393A>G (ATM) ENSP00000388058.2:p.Lys2465Glu
ENST00000713593.1:c.*6864A>G (ATM) ENSP00000518889.1:n.*6864A>G
ENST00000278616.9:c.7393A>G (ATM) ENSP00000278616.4:p.Lys2465Glu
ENST00000525056.2:n.1812A>G (ATM)
ENST00000525537.3:n.350A>G (ATM)
ENST00000638786.2:n.230A>G (ATM)
ENST00000682286.1:n.2150A>G (ATM)
ENST00000682302.1:n.1811A>G (ATM)
ENST00000683174.1:n.8877A>G (ATM)
ENST00000683524.1:n.2617A>G (ATM)
ENST00000684152.1:n.3107A>G (ATM)
ENST00000684447.1:n.1856A>G (ATM)
ENST00000527805.6:c.*2457A>G (ATM) ENSP00000435747.2:n.*2457A>G
ENST00000675595.1:c.*2528A>G (ATM) ENSP00000502563.1:n.*2528A>G
ENST00000675843.1:c.7393A>G (ATM) MANE Select ENSP00000501606.1:p.Lys2465Glu
ENST00000278616.8:c.7393A>G (ATM) ENSP00000278616.4:p.Lys2465Glu
ENST00000452508.6:c.7393A>G (ATM) ENSP00000388058.2:p.Lys2465Glu
ENST00000524792.5:n.3608A>G (ATM)
ENST00000525729.5:c.641-21228T>C (C11orf65) ENSP00000433395.1:n.641-21228T>C
ENST00000533690.5:n.2797A>G (ATM)
NM_000051.3:c.7393A>G , LRG_135t1:c.7393A>G (ATM) NP_000042.3:p.Lys2465Glu
XM_005271561.3:c.7393A>G (ATM) XP_005271618.2:p.Lys2465Glu
XM_005271562.3:c.7393A>G (ATM) XP_005271619.2:p.Lys2465Glu
XM_006718843.2:c.7393A>G (ATM) XP_006718906.1:p.Lys2465Glu
XM_006718845.1:c.3349A>G (ATM) XP_006718908.1:p.Lys1117Glu
XM_011542840.1:c.7393A>G (ATM) XP_011541142.1:p.Lys2465Glu
XM_011542841.1:c.7393A>G (ATM) XP_011541143.1:p.Lys2465Glu
XM_011542842.1:c.7228A>G (ATM) XP_011541144.1:p.Lys2410Glu
XM_011542843.1:c.7393A>G (ATM) XP_011541145.1:p.Lys2465Glu
XM_011542844.1:c.6349A>G (ATM) XP_011541146.1:p.Lys2117Glu
XM_011542845.1:c.6085A>G (ATM) XP_011541147.1:p.Lys2029Glu
XM_011542847.1:c.2464A>G (ATM) XP_011541149.1:p.Lys822Glu
NM_001330368.1:c.641-21228T>C (C11orf65) NP_001317297.1:n.641-21228T>C
NM_001351110.1:c.*38+4921T>C (C11orf65) NP_001338039.1:n.*38+4921T>C
NM_001351834.1:c.7393A>G (ATM) NP_001338763.1:p.Lys2465Glu
XM_005271562.5:c.7393A>G (ATM) XP_005271619.2:p.Lys2465Glu
XM_006718843.4:c.7393A>G (ATM) XP_006718906.1:p.Lys2465Glu
XM_006718845.2:c.3349A>G (ATM) XP_006718908.1:p.Lys1117Glu
XM_011542840.3:c.7393A>G (ATM) XP_011541142.1:p.Lys2465Glu
XM_011542842.3:c.7228A>G (ATM) XP_011541144.1:p.Lys2410Glu
XM_011542843.2:c.7393A>G (ATM) XP_011541145.1:p.Lys2465Glu
XM_011542844.3:c.6349A>G (ATM) XP_011541146.1:p.Lys2117Glu
XM_011542845.2:c.6085A>G (ATM) XP_011541147.1:p.Lys2029Glu
XM_017017789.2:c.7393A>G (ATM) XP_016873278.1:p.Lys2465Glu
XM_017017790.2:c.7393A>G (ATM) XP_016873279.1:p.Lys2465Glu
NM_001330368.2:c.641-21228T>C (C11orf65) NP_001317297.1:n.641-21228T>C
NM_001351110.2:c.*38+4921T>C (C11orf65) NP_001338039.1:n.*38+4921T>C
NM_001351834.2:c.7393A>G (ATM) NP_001338763.1:p.Lys2465Glu
NM_000051.4:c.7393A>G (ATM) MANE Select NP_000042.3:p.Lys2465Glu