Canonical Allele Identifier: CA382558739

Gene: ATM C11orf65

Linked Data

• dbSNP Id: rs1305313302
• gnomAD v4: 11-108327685-G-C
• MyVariant Identifiers: chr11:g.108198412G>C (hg19) ; chr11:g.108327685G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327685G>C , CM000673.2:g.108327685G>C	GRCh38
NC_000011.9:g.108198412G>C , CM000673.1:g.108198412G>C	GRCh37
NC_000011.8:g.107703622G>C	NCBI36
NG_009830.1:g.109854G>C , LRG_135:g.109854G>C
NG_054724.1:g.147148C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7016G>C (ATM)	ENSP00000388058.2:p.Arg2339Thr
ENST00000713593.1:c.*6487G>C (ATM)	ENSP00000518889.1:n.*6487G>C
ENST00000278616.9:c.7016G>C (ATM)	ENSP00000278616.4:p.Arg2339Thr
ENST00000525056.2:n.1435G>C (ATM)
ENST00000682286.1:n.1773G>C (ATM)
ENST00000682302.1:n.1434G>C (ATM)
ENST00000683174.1:n.8500G>C (ATM)
ENST00000683524.1:n.2240G>C (ATM)
ENST00000684152.1:n.2730G>C (ATM)
ENST00000684447.1:n.1479G>C (ATM)
ENST00000527805.6:c.*2080G>C (ATM)	ENSP00000435747.2:n.*2080G>C
ENST00000675595.1:c.*2151G>C (ATM)	ENSP00000502563.1:n.*2151G>C
ENST00000675843.1:c.7016G>C (ATM) MANE Select	ENSP00000501606.1:p.Arg2339Thr
ENST00000278616.8:c.7016G>C (ATM)	ENSP00000278616.4:p.Arg2339Thr
ENST00000452508.6:c.7016G>C (ATM)	ENSP00000388058.2:p.Arg2339Thr
ENST00000524792.5:n.3231G>C (ATM)
ENST00000525537.2:n.292G>C (ATM)
ENST00000525729.5:c.641-18614C>G (C11orf65)	ENSP00000433395.1:n.641-18614C>G
ENST00000527389.2:n.41G>C (ATM)
ENST00000533690.5:n.2420G>C (ATM)
NM_000051.3:c.7016G>C , LRG_135t1:c.7016G>C (ATM)	NP_000042.3:p.Arg2339Thr
XM_005271561.3:c.7016G>C (ATM)	XP_005271618.2:p.Arg2339Thr
XM_005271562.3:c.7016G>C (ATM)	XP_005271619.2:p.Arg2339Thr
XM_006718843.2:c.7016G>C (ATM)	XP_006718906.1:p.Arg2339Thr
XM_006718845.1:c.2972G>C (ATM)	XP_006718908.1:p.Arg991Thr
XM_011542840.1:c.7016G>C (ATM)	XP_011541142.1:p.Arg2339Thr
XM_011542841.1:c.7016G>C (ATM)	XP_011541143.1:p.Arg2339Thr
XM_011542842.1:c.6851G>C (ATM)	XP_011541144.1:p.Arg2284Thr
XM_011542843.1:c.7016G>C (ATM)	XP_011541145.1:p.Arg2339Thr
XM_011542844.1:c.5972G>C (ATM)	XP_011541146.1:p.Arg1991Thr
XM_011542845.1:c.5708G>C (ATM)	XP_011541147.1:p.Arg1903Thr
XM_011542847.1:c.2087G>C (ATM)	XP_011541149.1:p.Arg696Thr
NM_001330368.1:c.641-18614C>G (C11orf65)	NP_001317297.1:n.641-18614C>G
NM_001351110.1:c.*38+7535C>G (C11orf65)	NP_001338039.1:n.*38+7535C>G
NM_001351834.1:c.7016G>C (ATM)	NP_001338763.1:p.Arg2339Thr
XM_005271562.5:c.7016G>C (ATM)	XP_005271619.2:p.Arg2339Thr
XM_006718843.4:c.7016G>C (ATM)	XP_006718906.1:p.Arg2339Thr
XM_006718845.2:c.2972G>C (ATM)	XP_006718908.1:p.Arg991Thr
XM_011542840.3:c.7016G>C (ATM)	XP_011541142.1:p.Arg2339Thr
XM_011542842.3:c.6851G>C (ATM)	XP_011541144.1:p.Arg2284Thr
XM_011542843.2:c.7016G>C (ATM)	XP_011541145.1:p.Arg2339Thr
XM_011542844.3:c.5972G>C (ATM)	XP_011541146.1:p.Arg1991Thr
XM_011542845.2:c.5708G>C (ATM)	XP_011541147.1:p.Arg1903Thr
XM_017017789.2:c.7016G>C (ATM)	XP_016873278.1:p.Arg2339Thr
XM_017017790.2:c.7016G>C (ATM)	XP_016873279.1:p.Arg2339Thr
NM_001330368.2:c.641-18614C>G (C11orf65)	NP_001317297.1:n.641-18614C>G
NM_001351110.2:c.*38+7535C>G (C11orf65)	NP_001338039.1:n.*38+7535C>G
NM_001351834.2:c.7016G>C (ATM)	NP_001338763.1:p.Arg2339Thr
NM_000051.4:c.7016G>C (ATM) MANE Select	NP_000042.3:p.Arg2339Thr