Canonical Allele Identifier: CA382557010
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108326159G>T , CM000673.2:g.108326159G>T GRCh38
NC_000011.9:g.108196886G>T , CM000673.1:g.108196886G>T GRCh37
NC_000011.8:g.107702096G>T NCBI36
NG_009830.1:g.108328G>T , LRG_135:g.108328G>T
NG_054724.1:g.148674C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.6909G>T (ATM) ENSP00000388058.2:p.Lys2303Asn
ENST00000713593.1:c.*6380G>T (ATM) ENSP00000518889.1:n.*6380G>T
ENST00000278616.9:c.6909G>T (ATM) ENSP00000278616.4:p.Lys2303Asn
ENST00000525056.2:n.1328G>T (ATM)
ENST00000682286.1:n.1666G>T (ATM)
ENST00000682302.1:n.1327G>T (ATM)
ENST00000683174.1:n.8393G>T (ATM)
ENST00000683524.1:n.2133G>T (ATM)
ENST00000684152.1:n.2623G>T (ATM)
ENST00000527805.6:c.*1973G>T (ATM) ENSP00000435747.2:n.*1973G>T
ENST00000675595.1:c.*2044G>T (ATM) ENSP00000502563.1:n.*2044G>T
ENST00000675843.1:c.6909G>T (ATM) MANE Select ENSP00000501606.1:p.Lys2303Asn
ENST00000278616.8:c.6909G>T (ATM) ENSP00000278616.4:p.Lys2303Asn
ENST00000452508.6:c.6909G>T (ATM) ENSP00000388058.2:p.Lys2303Asn
ENST00000524792.5:n.3124G>T (ATM)
ENST00000525729.5:c.641-17088C>A (C11orf65) ENSP00000433395.1:n.641-17088C>A
ENST00000533690.5:n.2313G>T (ATM)
NM_000051.3:c.6909G>T , LRG_135t1:c.6909G>T (ATM) NP_000042.3:p.Lys2303Asn
XM_005271561.3:c.6909G>T (ATM) XP_005271618.2:p.Lys2303Asn
XM_005271562.3:c.6909G>T (ATM) XP_005271619.2:p.Lys2303Asn
XM_006718843.2:c.6909G>T (ATM) XP_006718906.1:p.Lys2303Asn
XM_006718845.1:c.2865G>T (ATM) XP_006718908.1:p.Lys955Asn
XM_011542840.1:c.6909G>T (ATM) XP_011541142.1:p.Lys2303Asn
XM_011542841.1:c.6909G>T (ATM) XP_011541143.1:p.Lys2303Asn
XM_011542842.1:c.6744G>T (ATM) XP_011541144.1:p.Lys2248Asn
XM_011542843.1:c.6909G>T (ATM) XP_011541145.1:p.Lys2303Asn
XM_011542844.1:c.5865G>T (ATM) XP_011541146.1:p.Lys1955Asn
XM_011542845.1:c.5601G>T (ATM) XP_011541147.1:p.Lys1867Asn
XM_011542847.1:c.1980G>T (ATM) XP_011541149.1:p.Lys660Asn
NM_001330368.1:c.641-17088C>A (C11orf65) NP_001317297.1:n.641-17088C>A
NM_001351110.1:c.*38+9061C>A (C11orf65) NP_001338039.1:n.*38+9061C>A
NM_001351834.1:c.6909G>T (ATM) NP_001338763.1:p.Lys2303Asn
XM_005271562.5:c.6909G>T (ATM) XP_005271619.2:p.Lys2303Asn
XM_006718843.4:c.6909G>T (ATM) XP_006718906.1:p.Lys2303Asn
XM_006718845.2:c.2865G>T (ATM) XP_006718908.1:p.Lys955Asn
XM_011542840.3:c.6909G>T (ATM) XP_011541142.1:p.Lys2303Asn
XM_011542842.3:c.6744G>T (ATM) XP_011541144.1:p.Lys2248Asn
XM_011542843.2:c.6909G>T (ATM) XP_011541145.1:p.Lys2303Asn
XM_011542844.3:c.5865G>T (ATM) XP_011541146.1:p.Lys1955Asn
XM_011542845.2:c.5601G>T (ATM) XP_011541147.1:p.Lys1867Asn
XM_017017789.2:c.6909G>T (ATM) XP_016873278.1:p.Lys2303Asn
XM_017017790.2:c.6909G>T (ATM) XP_016873279.1:p.Lys2303Asn
NM_001330368.2:c.641-17088C>A (C11orf65) NP_001317297.1:n.641-17088C>A
NM_001351110.2:c.*38+9061C>A (C11orf65) NP_001338039.1:n.*38+9061C>A
NM_001351834.2:c.6909G>T (ATM) NP_001338763.1:p.Lys2303Asn
NM_000051.4:c.6909G>T (ATM) MANE Select NP_000042.3:p.Lys2303Asn