Canonical Allele Identifier: CA476745417

Gene: ATM C11orf65

Linked Data

• MyVariant Identifiers: chr11:g.108196154T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108325427T>C , CM000673.2:g.108325427T>C	GRCh38
NC_000011.9:g.108196154T>C , CM000673.1:g.108196154T>C	GRCh37
NC_000011.8:g.107701364T>C	NCBI36
NG_009830.1:g.107596T>C , LRG_135:g.107596T>C
NG_054724.1:g.149406A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6690T>C (ATM)	ENSP00000388058.2:p.Ile2230=
ENST00000713593.1:c.*6161T>C (ATM)	ENSP00000518889.1:n.*6161T>C
ENST00000278616.9:c.6690T>C (ATM)	ENSP00000278616.4:p.Ile2230=
ENST00000525056.2:n.1109T>C (ATM)
ENST00000682286.1:n.1447T>C (ATM)
ENST00000682302.1:n.1108T>C (ATM)
ENST00000683174.1:n.8174T>C (ATM)
ENST00000683524.1:n.1914T>C (ATM)
ENST00000684152.1:n.2404T>C (ATM)
ENST00000527805.6:c.*1754T>C (ATM)	ENSP00000435747.2:n.*1754T>C
ENST00000675595.1:c.*1825T>C (ATM)	ENSP00000502563.1:n.*1825T>C
ENST00000675843.1:c.6690T>C (ATM) MANE Select	ENSP00000501606.1:p.Ile2230=
ENST00000278616.8:c.6690T>C (ATM)	ENSP00000278616.4:p.Ile2230=
ENST00000452508.6:c.6690T>C (ATM)	ENSP00000388058.2:p.Ile2230=
ENST00000524792.5:n.2905T>C (ATM)
ENST00000525729.5:c.641-16356A>G (C11orf65)	ENSP00000433395.1:n.641-16356A>G
ENST00000533690.5:n.2094T>C (ATM)
NM_000051.3:c.6690T>C , LRG_135t1:c.6690T>C (ATM)	NP_000042.3:p.Ile2230=
XM_005271561.3:c.6690T>C (ATM)	XP_005271618.2:p.Ile2230=
XM_005271562.3:c.6690T>C (ATM)	XP_005271619.2:p.Ile2230=
XM_006718843.2:c.6690T>C (ATM)	XP_006718906.1:p.Ile2230=
XM_006718845.1:c.2646T>C (ATM)	XP_006718908.1:p.Ile882=
XM_011542840.1:c.6690T>C (ATM)	XP_011541142.1:p.Ile2230=
XM_011542841.1:c.6690T>C (ATM)	XP_011541143.1:p.Ile2230=
XM_011542842.1:c.6525T>C (ATM)	XP_011541144.1:p.Ile2175=
XM_011542843.1:c.6690T>C (ATM)	XP_011541145.1:p.Ile2230=
XM_011542844.1:c.5646T>C (ATM)	XP_011541146.1:p.Ile1882=
XM_011542845.1:c.5382T>C (ATM)	XP_011541147.1:p.Ile1794=
XM_011542847.1:c.1761T>C (ATM)	XP_011541149.1:p.Ile587=
NM_001330368.1:c.641-16356A>G (C11orf65)	NP_001317297.1:n.641-16356A>G
NM_001351110.1:c.*38+9793A>G (C11orf65)	NP_001338039.1:n.*38+9793A>G
NM_001351834.1:c.6690T>C (ATM)	NP_001338763.1:p.Ile2230=
XM_005271562.5:c.6690T>C (ATM)	XP_005271619.2:p.Ile2230=
XM_006718843.4:c.6690T>C (ATM)	XP_006718906.1:p.Ile2230=
XM_006718845.2:c.2646T>C (ATM)	XP_006718908.1:p.Ile882=
XM_011542840.3:c.6690T>C (ATM)	XP_011541142.1:p.Ile2230=
XM_011542842.3:c.6525T>C (ATM)	XP_011541144.1:p.Ile2175=
XM_011542843.2:c.6690T>C (ATM)	XP_011541145.1:p.Ile2230=
XM_011542844.3:c.5646T>C (ATM)	XP_011541146.1:p.Ile1882=
XM_011542845.2:c.5382T>C (ATM)	XP_011541147.1:p.Ile1794=
XM_017017789.2:c.6690T>C (ATM)	XP_016873278.1:p.Ile2230=
XM_017017790.2:c.6690T>C (ATM)	XP_016873279.1:p.Ile2230=
NM_001330368.2:c.641-16356A>G (C11orf65)	NP_001317297.1:n.641-16356A>G
NM_001351110.2:c.*38+9793A>G (C11orf65)	NP_001338039.1:n.*38+9793A>G
NM_001351834.2:c.6690T>C (ATM)	NP_001338763.1:p.Ile2230=
NM_000051.4:c.6690T>C (ATM) MANE Select	NP_000042.3:p.Ile2230=