Canonical Allele Identifier: CA476676516

Gene: ATM C11orf65

Linked Data

• MyVariant Identifiers: chr11:g.108198473C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108327746C>G , CM000673.2:g.108327746C>G	GRCh38
NC_000011.9:g.108198473C>G , CM000673.1:g.108198473C>G	GRCh37
NC_000011.8:g.107703683C>G	NCBI36
NG_009830.1:g.109915C>G , LRG_135:g.109915C>G
NG_054724.1:g.147087G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7077C>G (ATM)	ENSP00000388058.2:p.Thr2359=
ENST00000713593.1:c.*6548C>G (ATM)	ENSP00000518889.1:n.*6548C>G
ENST00000278616.9:c.7077C>G (ATM)	ENSP00000278616.4:p.Thr2359=
ENST00000525056.2:n.1496C>G (ATM)
ENST00000525537.3:n.34C>G (ATM)
ENST00000682286.1:n.1834C>G (ATM)
ENST00000682302.1:n.1495C>G (ATM)
ENST00000683174.1:n.8561C>G (ATM)
ENST00000683524.1:n.2301C>G (ATM)
ENST00000684152.1:n.2791C>G (ATM)
ENST00000684447.1:n.1540C>G (ATM)
ENST00000527805.6:c.*2141C>G (ATM)	ENSP00000435747.2:n.*2141C>G
ENST00000675595.1:c.*2212C>G (ATM)	ENSP00000502563.1:n.*2212C>G
ENST00000675843.1:c.7077C>G (ATM) MANE Select	ENSP00000501606.1:p.Thr2359=
ENST00000278616.8:c.7077C>G (ATM)	ENSP00000278616.4:p.Thr2359=
ENST00000452508.6:c.7077C>G (ATM)	ENSP00000388058.2:p.Thr2359=
ENST00000524792.5:n.3292C>G (ATM)
ENST00000525537.2:n.353C>G (ATM)
ENST00000525729.5:c.641-18675G>C (C11orf65)	ENSP00000433395.1:n.641-18675G>C
ENST00000527389.2:n.102C>G (ATM)
ENST00000533690.5:n.2481C>G (ATM)
NM_000051.3:c.7077C>G , LRG_135t1:c.7077C>G (ATM)	NP_000042.3:p.Thr2359=
XM_005271561.3:c.7077C>G (ATM)	XP_005271618.2:p.Thr2359=
XM_005271562.3:c.7077C>G (ATM)	XP_005271619.2:p.Thr2359=
XM_006718843.2:c.7077C>G (ATM)	XP_006718906.1:p.Thr2359=
XM_006718845.1:c.3033C>G (ATM)	XP_006718908.1:p.Thr1011=
XM_011542840.1:c.7077C>G (ATM)	XP_011541142.1:p.Thr2359=
XM_011542841.1:c.7077C>G (ATM)	XP_011541143.1:p.Thr2359=
XM_011542842.1:c.6912C>G (ATM)	XP_011541144.1:p.Thr2304=
XM_011542843.1:c.7077C>G (ATM)	XP_011541145.1:p.Thr2359=
XM_011542844.1:c.6033C>G (ATM)	XP_011541146.1:p.Thr2011=
XM_011542845.1:c.5769C>G (ATM)	XP_011541147.1:p.Thr1923=
XM_011542847.1:c.2148C>G (ATM)	XP_011541149.1:p.Thr716=
NM_001330368.1:c.641-18675G>C (C11orf65)	NP_001317297.1:n.641-18675G>C
NM_001351110.1:c.*38+7474G>C (C11orf65)	NP_001338039.1:n.*38+7474G>C
NM_001351834.1:c.7077C>G (ATM)	NP_001338763.1:p.Thr2359=
XM_005271562.5:c.7077C>G (ATM)	XP_005271619.2:p.Thr2359=
XM_006718843.4:c.7077C>G (ATM)	XP_006718906.1:p.Thr2359=
XM_006718845.2:c.3033C>G (ATM)	XP_006718908.1:p.Thr1011=
XM_011542840.3:c.7077C>G (ATM)	XP_011541142.1:p.Thr2359=
XM_011542842.3:c.6912C>G (ATM)	XP_011541144.1:p.Thr2304=
XM_011542843.2:c.7077C>G (ATM)	XP_011541145.1:p.Thr2359=
XM_011542844.3:c.6033C>G (ATM)	XP_011541146.1:p.Thr2011=
XM_011542845.2:c.5769C>G (ATM)	XP_011541147.1:p.Thr1923=
XM_017017789.2:c.7077C>G (ATM)	XP_016873278.1:p.Thr2359=
XM_017017790.2:c.7077C>G (ATM)	XP_016873279.1:p.Thr2359=
NM_001330368.2:c.641-18675G>C (C11orf65)	NP_001317297.1:n.641-18675G>C
NM_001351110.2:c.*38+7474G>C (C11orf65)	NP_001338039.1:n.*38+7474G>C
NM_001351834.2:c.7077C>G (ATM)	NP_001338763.1:p.Thr2359=
NM_000051.4:c.7077C>G (ATM) MANE Select	NP_000042.3:p.Thr2359=