Canonical Allele Identifier: CA382556745

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 848073
• ClinVar RCV Id: RCV001051753 ; RCV002365696
• dbSNP Id: rs2085653356
• gnomAD v4: 11-108326115-T-C
• MyVariant Identifiers: chr11:g.108196842T>C (hg19) ; chr11:g.108326115T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108326115T>C , CM000673.2:g.108326115T>C	GRCh38
NC_000011.9:g.108196842T>C , CM000673.1:g.108196842T>C	GRCh37
NC_000011.8:g.107702052T>C	NCBI36
NG_009830.1:g.108284T>C , LRG_135:g.108284T>C
NG_054724.1:g.148718A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6865T>C (ATM)	ENSP00000388058.2:p.Ser2289Pro
ENST00000713593.1:c.*6336T>C (ATM)	ENSP00000518889.1:n.*6336T>C
ENST00000278616.9:c.6865T>C (ATM)	ENSP00000278616.4:p.Ser2289Pro
ENST00000525056.2:n.1284T>C (ATM)
ENST00000682286.1:n.1622T>C (ATM)
ENST00000682302.1:n.1283T>C (ATM)
ENST00000683174.1:n.8349T>C (ATM)
ENST00000683524.1:n.2089T>C (ATM)
ENST00000684152.1:n.2579T>C (ATM)
ENST00000527805.6:c.*1929T>C (ATM)	ENSP00000435747.2:n.*1929T>C
ENST00000675595.1:c.*2000T>C (ATM)	ENSP00000502563.1:n.*2000T>C
ENST00000675843.1:c.6865T>C (ATM) MANE Select	ENSP00000501606.1:p.Ser2289Pro
ENST00000278616.8:c.6865T>C (ATM)	ENSP00000278616.4:p.Ser2289Pro
ENST00000452508.6:c.6865T>C (ATM)	ENSP00000388058.2:p.Ser2289Pro
ENST00000524792.5:n.3080T>C (ATM)
ENST00000525729.5:c.641-17044A>G (C11orf65)	ENSP00000433395.1:n.641-17044A>G
ENST00000533690.5:n.2269T>C (ATM)
NM_000051.3:c.6865T>C , LRG_135t1:c.6865T>C (ATM)	NP_000042.3:p.Ser2289Pro
XM_005271561.3:c.6865T>C (ATM)	XP_005271618.2:p.Ser2289Pro
XM_005271562.3:c.6865T>C (ATM)	XP_005271619.2:p.Ser2289Pro
XM_006718843.2:c.6865T>C (ATM)	XP_006718906.1:p.Ser2289Pro
XM_006718845.1:c.2821T>C (ATM)	XP_006718908.1:p.Ser941Pro
XM_011542840.1:c.6865T>C (ATM)	XP_011541142.1:p.Ser2289Pro
XM_011542841.1:c.6865T>C (ATM)	XP_011541143.1:p.Ser2289Pro
XM_011542842.1:c.6700T>C (ATM)	XP_011541144.1:p.Ser2234Pro
XM_011542843.1:c.6865T>C (ATM)	XP_011541145.1:p.Ser2289Pro
XM_011542844.1:c.5821T>C (ATM)	XP_011541146.1:p.Ser1941Pro
XM_011542845.1:c.5557T>C (ATM)	XP_011541147.1:p.Ser1853Pro
XM_011542847.1:c.1936T>C (ATM)	XP_011541149.1:p.Ser646Pro
NM_001330368.1:c.641-17044A>G (C11orf65)	NP_001317297.1:n.641-17044A>G
NM_001351110.1:c.*38+9105A>G (C11orf65)	NP_001338039.1:n.*38+9105A>G
NM_001351834.1:c.6865T>C (ATM)	NP_001338763.1:p.Ser2289Pro
XM_005271562.5:c.6865T>C (ATM)	XP_005271619.2:p.Ser2289Pro
XM_006718843.4:c.6865T>C (ATM)	XP_006718906.1:p.Ser2289Pro
XM_006718845.2:c.2821T>C (ATM)	XP_006718908.1:p.Ser941Pro
XM_011542840.3:c.6865T>C (ATM)	XP_011541142.1:p.Ser2289Pro
XM_011542842.3:c.6700T>C (ATM)	XP_011541144.1:p.Ser2234Pro
XM_011542843.2:c.6865T>C (ATM)	XP_011541145.1:p.Ser2289Pro
XM_011542844.3:c.5821T>C (ATM)	XP_011541146.1:p.Ser1941Pro
XM_011542845.2:c.5557T>C (ATM)	XP_011541147.1:p.Ser1853Pro
XM_017017789.2:c.6865T>C (ATM)	XP_016873278.1:p.Ser2289Pro
XM_017017790.2:c.6865T>C (ATM)	XP_016873279.1:p.Ser2289Pro
NM_001330368.2:c.641-17044A>G (C11orf65)	NP_001317297.1:n.641-17044A>G
NM_001351110.2:c.*38+9105A>G (C11orf65)	NP_001338039.1:n.*38+9105A>G
NM_001351834.2:c.6865T>C (ATM)	NP_001338763.1:p.Ser2289Pro
NM_000051.4:c.6865T>C (ATM) MANE Select	NP_000042.3:p.Ser2289Pro