Canonical Allele Identifier: CA382559857

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 482659
• ClinVar RCV Id: RCV000566704 ; RCV001858241 ; RCV003465226
• dbSNP Id: rs1555122941
• gnomAD v4: 11-108330213-G-C
• MyVariant Identifiers: chr11:g.108200940G>C (hg19) ; chr11:g.108330213G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108330213G>C , CM000673.2:g.108330213G>C	GRCh38
NC_000011.9:g.108200940G>C , CM000673.1:g.108200940G>C	GRCh37
NC_000011.8:g.107706150G>C	NCBI36
NG_009830.1:g.112382G>C , LRG_135:g.112382G>C
NG_054724.1:g.144620C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7308-1G>C (ATM)	ENSP00000388058.2:n.7308-1G>C
ENST00000713593.1:c.*6779-1G>C (ATM)	ENSP00000518889.1:n.*6779-1G>C
ENST00000278616.9:c.7308-1G>C (ATM)	ENSP00000278616.4:n.7308-1G>C
ENST00000525056.2:n.1727-1G>C (ATM)
ENST00000525537.3:n.265-1G>C (ATM)
ENST00000638786.2:n.145-1G>C (ATM)
ENST00000682286.1:n.2065-1G>C (ATM)
ENST00000682302.1:n.1726-1G>C (ATM)
ENST00000683174.1:n.8792-1G>C (ATM)
ENST00000683524.1:n.2532-1G>C (ATM)
ENST00000684152.1:n.3022-1G>C (ATM)
ENST00000684447.1:n.1771-1G>C (ATM)
ENST00000527805.6:c.*2372-1G>C (ATM)	ENSP00000435747.2:n.*2372-1G>C
ENST00000675595.1:c.*2443-1G>C (ATM)	ENSP00000502563.1:n.*2443-1G>C
ENST00000675843.1:c.7308-1G>C (ATM) MANE Select	ENSP00000501606.1:n.7308-1G>C
ENST00000278616.8:c.7308-1G>C (ATM)	ENSP00000278616.4:n.7308-1G>C
ENST00000452508.6:c.7308-1G>C (ATM)	ENSP00000388058.2:n.7308-1G>C
ENST00000524792.5:n.3523-1G>C (ATM)
ENST00000525729.5:c.641-21142C>G (C11orf65)	ENSP00000433395.1:n.641-21142C>G
ENST00000533690.5:n.2712-1G>C (ATM)
NM_000051.3:c.7308-1G>C , LRG_135t1:c.7308-1G>C (ATM)	NP_000042.3:n.7308-1G>C
XM_005271561.3:c.7308-1G>C (ATM)	XP_005271618.2:n.7308-1G>C
XM_005271562.3:c.7308-1G>C (ATM)	XP_005271619.2:n.7308-1G>C
XM_006718843.2:c.7308-1G>C (ATM)	XP_006718906.1:n.7308-1G>C
XM_006718845.1:c.3264-1G>C (ATM)	XP_006718908.1:n.3264-1G>C
XM_011542840.1:c.7308-1G>C (ATM)	XP_011541142.1:n.7308-1G>C
XM_011542841.1:c.7308-1G>C (ATM)	XP_011541143.1:n.7308-1G>C
XM_011542842.1:c.7143-1G>C (ATM)	XP_011541144.1:n.7143-1G>C
XM_011542843.1:c.7308-1G>C (ATM)	XP_011541145.1:n.7308-1G>C
XM_011542844.1:c.6264-1G>C (ATM)	XP_011541146.1:n.6264-1G>C
XM_011542845.1:c.6000-1G>C (ATM)	XP_011541147.1:n.6000-1G>C
XM_011542847.1:c.2379-1G>C (ATM)	XP_011541149.1:n.2379-1G>C
NM_001330368.1:c.641-21142C>G (C11orf65)	NP_001317297.1:n.641-21142C>G
NM_001351110.1:c.*38+5007C>G (C11orf65)	NP_001338039.1:n.*38+5007C>G
NM_001351834.1:c.7308-1G>C (ATM)	NP_001338763.1:n.7308-1G>C
XM_005271562.5:c.7308-1G>C (ATM)	XP_005271619.2:n.7308-1G>C
XM_006718843.4:c.7308-1G>C (ATM)	XP_006718906.1:n.7308-1G>C
XM_006718845.2:c.3264-1G>C (ATM)	XP_006718908.1:n.3264-1G>C
XM_011542840.3:c.7308-1G>C (ATM)	XP_011541142.1:n.7308-1G>C
XM_011542842.3:c.7143-1G>C (ATM)	XP_011541144.1:n.7143-1G>C
XM_011542843.2:c.7308-1G>C (ATM)	XP_011541145.1:n.7308-1G>C
XM_011542844.3:c.6264-1G>C (ATM)	XP_011541146.1:n.6264-1G>C
XM_011542845.2:c.6000-1G>C (ATM)	XP_011541147.1:n.6000-1G>C
XM_017017789.2:c.7308-1G>C (ATM)	XP_016873278.1:n.7308-1G>C
XM_017017790.2:c.7308-1G>C (ATM)	XP_016873279.1:n.7308-1G>C
NM_001330368.2:c.641-21142C>G (C11orf65)	NP_001317297.1:n.641-21142C>G
NM_001351110.2:c.*38+5007C>G (C11orf65)	NP_001338039.1:n.*38+5007C>G
NM_001351834.2:c.7308-1G>C (ATM)	NP_001338763.1:n.7308-1G>C
NM_000051.4:c.7308-1G>C (ATM) MANE Select	NP_000042.3:n.7308-1G>C