Canonical Allele Identifier: CA1998811016
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108329229A= , CM000673.2:g.108329229A= GRCh38
NC_000011.9:g.108199956A= , CM000673.1:g.108199956A= GRCh37
NC_000011.8:g.107705166A= NCBI36
NG_009830.1:g.111398A= , LRG_135:g.111398A=
NG_054724.1:g.145604T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.7298A= (ATM) ENSP00000388058.2:p.Gln2433=
ENST00000713593.1:c.*6769A= (ATM) ENSP00000518889.1:n.*6769A=
ENST00000278616.9:c.7298A= (ATM) ENSP00000278616.4:p.Gln2433=
ENST00000525056.2:n.1717A= (ATM)
ENST00000525537.3:n.255A= (ATM)
ENST00000638786.2:n.135A= (ATM)
ENST00000682286.1:n.2055A= (ATM)
ENST00000682302.1:n.1716A= (ATM)
ENST00000683174.1:n.8782A= (ATM)
ENST00000683524.1:n.2522A= (ATM)
ENST00000684152.1:n.3012A= (ATM)
ENST00000684447.1:n.1761A= (ATM)
ENST00000527805.6:c.*2362A= (ATM) ENSP00000435747.2:n.*2362A=
ENST00000675595.1:c.*2433A= (ATM) ENSP00000502563.1:n.*2433A=
ENST00000675843.1:c.7298A= (ATM) MANE Select ENSP00000501606.1:p.Gln2433=
ENST00000278616.8:c.7298A= (ATM) ENSP00000278616.4:p.Gln2433=
ENST00000452508.6:c.7298A= (ATM) ENSP00000388058.2:p.Gln2433=
ENST00000524792.5:n.3513A= (ATM)
ENST00000525537.2:n.574A= (ATM)
ENST00000525729.5:c.641-20158T= (C11orf65) ENSP00000433395.1:n.641-20158T=
ENST00000527389.2:n.323A= (ATM)
ENST00000533690.5:n.2702A= (ATM)
NM_000051.3:c.7298A= , LRG_135t1:c.7298A= (ATM) NP_000042.3:p.Gln2433=
XM_005271561.3:c.7298A= (ATM) XP_005271618.2:p.Gln2433=
XM_005271562.3:c.7298A= (ATM) XP_005271619.2:p.Gln2433=
XM_006718843.2:c.7298A= (ATM) XP_006718906.1:p.Gln2433=
XM_006718845.1:c.3254A= (ATM) XP_006718908.1:p.Gln1085=
XM_011542840.1:c.7298A= (ATM) XP_011541142.1:p.Gln2433=
XM_011542841.1:c.7298A= (ATM) XP_011541143.1:p.Gln2433=
XM_011542842.1:c.7133A= (ATM) XP_011541144.1:p.Gln2378=
XM_011542843.1:c.7298A= (ATM) XP_011541145.1:p.Gln2433=
XM_011542844.1:c.6254A= (ATM) XP_011541146.1:p.Gln2085=
XM_011542845.1:c.5990A= (ATM) XP_011541147.1:p.Gln1997=
XM_011542847.1:c.2369A= (ATM) XP_011541149.1:p.Gln790=
NM_001330368.1:c.641-20158T= (C11orf65) NP_001317297.1:n.641-20158T=
NM_001351110.1:c.*38+5991T= (C11orf65) NP_001338039.1:n.*38+5991T=
NM_001351834.1:c.7298A= (ATM) NP_001338763.1:p.Gln2433=
XM_005271562.5:c.7298A= (ATM) XP_005271619.2:p.Gln2433=
XM_006718843.4:c.7298A= (ATM) XP_006718906.1:p.Gln2433=
XM_006718845.2:c.3254A= (ATM) XP_006718908.1:p.Gln1085=
XM_011542840.3:c.7298A= (ATM) XP_011541142.1:p.Gln2433=
XM_011542842.3:c.7133A= (ATM) XP_011541144.1:p.Gln2378=
XM_011542843.2:c.7298A= (ATM) XP_011541145.1:p.Gln2433=
XM_011542844.3:c.6254A= (ATM) XP_011541146.1:p.Gln2085=
XM_011542845.2:c.5990A= (ATM) XP_011541147.1:p.Gln1997=
XM_017017789.2:c.7298A= (ATM) XP_016873278.1:p.Gln2433=
XM_017017790.2:c.7298A= (ATM) XP_016873279.1:p.Gln2433=
NM_001330368.2:c.641-20158T= (C11orf65) NP_001317297.1:n.641-20158T=
NM_001351110.2:c.*38+5991T= (C11orf65) NP_001338039.1:n.*38+5991T=
NM_001351834.2:c.7298A= (ATM) NP_001338763.1:p.Gln2433=
NM_000051.4:c.7298A= (ATM) MANE Select NP_000042.3:p.Gln2433=