Canonical Allele Identifier: CA476676174

Gene: ATM C11orf65

Linked Data

• dbSNP Id: rs746514937
• MyVariant Identifiers: chr11:g.108192073G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108321346G>C , CM000673.2:g.108321346G>C	GRCh38
NC_000011.9:g.108192073G>C , CM000673.1:g.108192073G>C	GRCh37
NC_000011.8:g.107697283G>C	NCBI36
NG_009830.1:g.103515G>C , LRG_135:g.103515G>C
NG_054724.1:g.153487C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.6498G>C (ATM)	ENSP00000388058.2:p.Val2166=
ENST00000713593.1:c.*5969G>C (ATM)	ENSP00000518889.1:n.*5969G>C
ENST00000278616.9:c.6498G>C (ATM)	ENSP00000278616.4:p.Val2166=
ENST00000525056.2:n.917G>C (ATM)
ENST00000682286.1:n.1255G>C (ATM)
ENST00000682302.1:n.916G>C (ATM)
ENST00000683174.1:n.7982G>C (ATM)
ENST00000683524.1:n.1722G>C (ATM)
ENST00000684152.1:n.2212G>C (ATM)
ENST00000527805.6:c.*1562G>C (ATM)	ENSP00000435747.2:n.*1562G>C
ENST00000675595.1:c.*1633G>C (ATM)	ENSP00000502563.1:n.*1633G>C
ENST00000675843.1:c.6498G>C (ATM) MANE Select	ENSP00000501606.1:p.Val2166=
ENST00000278616.8:c.6498G>C (ATM)	ENSP00000278616.4:p.Val2166=
ENST00000452508.6:c.6498G>C (ATM)	ENSP00000388058.2:p.Val2166=
ENST00000524792.5:n.2713G>C (ATM)
ENST00000525729.5:c.641-12275C>G (C11orf65)	ENSP00000433395.1:n.641-12275C>G
ENST00000533690.5:n.1902G>C (ATM)
NM_000051.3:c.6498G>C , LRG_135t1:c.6498G>C (ATM)	NP_000042.3:p.Val2166=
XM_005271561.3:c.6498G>C (ATM)	XP_005271618.2:p.Val2166=
XM_005271562.3:c.6498G>C (ATM)	XP_005271619.2:p.Val2166=
XM_006718843.2:c.6498G>C (ATM)	XP_006718906.1:p.Val2166=
XM_006718845.1:c.2454G>C (ATM)	XP_006718908.1:p.Val818=
XM_011542840.1:c.6498G>C (ATM)	XP_011541142.1:p.Val2166=
XM_011542841.1:c.6498G>C (ATM)	XP_011541143.1:p.Val2166=
XM_011542842.1:c.6333G>C (ATM)	XP_011541144.1:p.Val2111=
XM_011542843.1:c.6498G>C (ATM)	XP_011541145.1:p.Val2166=
XM_011542844.1:c.5454G>C (ATM)	XP_011541146.1:p.Val1818=
XM_011542845.1:c.5190G>C (ATM)	XP_011541147.1:p.Val1730=
XM_011542847.1:c.1569G>C (ATM)	XP_011541149.1:p.Val523=
NM_001330368.1:c.641-12275C>G (C11orf65)	NP_001317297.1:n.641-12275C>G
NM_001351110.1:c.*39-12275C>G (C11orf65)	NP_001338039.1:n.*39-12275C>G
NM_001351834.1:c.6498G>C (ATM)	NP_001338763.1:p.Val2166=
XM_005271562.5:c.6498G>C (ATM)	XP_005271619.2:p.Val2166=
XM_006718843.4:c.6498G>C (ATM)	XP_006718906.1:p.Val2166=
XM_006718845.2:c.2454G>C (ATM)	XP_006718908.1:p.Val818=
XM_011542840.3:c.6498G>C (ATM)	XP_011541142.1:p.Val2166=
XM_011542842.3:c.6333G>C (ATM)	XP_011541144.1:p.Val2111=
XM_011542843.2:c.6498G>C (ATM)	XP_011541145.1:p.Val2166=
XM_011542844.3:c.5454G>C (ATM)	XP_011541146.1:p.Val1818=
XM_011542845.2:c.5190G>C (ATM)	XP_011541147.1:p.Val1730=
XM_017017789.2:c.6498G>C (ATM)	XP_016873278.1:p.Val2166=
XM_017017790.2:c.6498G>C (ATM)	XP_016873279.1:p.Val2166=
NM_001330368.2:c.641-12275C>G (C11orf65)	NP_001317297.1:n.641-12275C>G
NM_001351110.2:c.*39-12275C>G (C11orf65)	NP_001338039.1:n.*39-12275C>G
NM_001351834.2:c.6498G>C (ATM)	NP_001338763.1:p.Val2166=
NM_000051.4:c.6498G>C (ATM) MANE Select	NP_000042.3:p.Val2166=