Canonical Allele Identifier: CA6265967

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 1109055
• ClinVar RCV Id: RCV001434755
• dbSNP Id: rs756551824
• ExAC: 11:108192121 G / A
• gnomAD v2: 11-108192121-G-A
• gnomAD v4: 11-108321394-G-A
• MyVariant Identifiers: chr11:g.108192121G>A (hg19) ; chr11:g.108321394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108321394G>A , CM000673.2:g.108321394G>A	GRCh38
NC_000011.9:g.108192121G>A , CM000673.1:g.108192121G>A	GRCh37
NC_000011.8:g.107697331G>A	NCBI36
NG_009830.1:g.103563G>A , LRG_135:g.103563G>A
NG_054724.1:g.153439C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6546G>A (ATM)	ENSP00000388058.2:p.Leu2182=
ENST00000713593.1:c.*6017G>A (ATM)	ENSP00000518889.1:n.*6017G>A
ENST00000278616.9:c.6546G>A (ATM)	ENSP00000278616.4:p.Leu2182=
ENST00000525056.2:n.965G>A (ATM)
ENST00000682286.1:n.1303G>A (ATM)
ENST00000682302.1:n.964G>A (ATM)
ENST00000683174.1:n.8030G>A (ATM)
ENST00000683524.1:n.1770G>A (ATM)
ENST00000684152.1:n.2260G>A (ATM)
ENST00000527805.6:c.*1610G>A (ATM)	ENSP00000435747.2:n.*1610G>A
ENST00000675595.1:c.*1681G>A (ATM)	ENSP00000502563.1:n.*1681G>A
ENST00000675843.1:c.6546G>A (ATM) MANE Select	ENSP00000501606.1:p.Leu2182=
ENST00000278616.8:c.6546G>A (ATM)	ENSP00000278616.4:p.Leu2182=
ENST00000452508.6:c.6546G>A (ATM)	ENSP00000388058.2:p.Leu2182=
ENST00000524792.5:n.2761G>A (ATM)
ENST00000525729.5:c.641-12323C>T (C11orf65)	ENSP00000433395.1:n.641-12323C>T
ENST00000533690.5:n.1950G>A (ATM)
NM_000051.3:c.6546G>A , LRG_135t1:c.6546G>A (ATM)	NP_000042.3:p.Leu2182=
XM_005271561.3:c.6546G>A (ATM)	XP_005271618.2:p.Leu2182=
XM_005271562.3:c.6546G>A (ATM)	XP_005271619.2:p.Leu2182=
XM_006718843.2:c.6546G>A (ATM)	XP_006718906.1:p.Leu2182=
XM_006718845.1:c.2502G>A (ATM)	XP_006718908.1:p.Leu834=
XM_011542840.1:c.6546G>A (ATM)	XP_011541142.1:p.Leu2182=
XM_011542841.1:c.6546G>A (ATM)	XP_011541143.1:p.Leu2182=
XM_011542842.1:c.6381G>A (ATM)	XP_011541144.1:p.Leu2127=
XM_011542843.1:c.6546G>A (ATM)	XP_011541145.1:p.Leu2182=
XM_011542844.1:c.5502G>A (ATM)	XP_011541146.1:p.Leu1834=
XM_011542845.1:c.5238G>A (ATM)	XP_011541147.1:p.Leu1746=
XM_011542847.1:c.1617G>A (ATM)	XP_011541149.1:p.Leu539=
NM_001330368.1:c.641-12323C>T (C11orf65)	NP_001317297.1:n.641-12323C>T
NM_001351110.1:c.*39-12323C>T (C11orf65)	NP_001338039.1:n.*39-12323C>T
NM_001351834.1:c.6546G>A (ATM)	NP_001338763.1:p.Leu2182=
XM_005271562.5:c.6546G>A (ATM)	XP_005271619.2:p.Leu2182=
XM_006718843.4:c.6546G>A (ATM)	XP_006718906.1:p.Leu2182=
XM_006718845.2:c.2502G>A (ATM)	XP_006718908.1:p.Leu834=
XM_011542840.3:c.6546G>A (ATM)	XP_011541142.1:p.Leu2182=
XM_011542842.3:c.6381G>A (ATM)	XP_011541144.1:p.Leu2127=
XM_011542843.2:c.6546G>A (ATM)	XP_011541145.1:p.Leu2182=
XM_011542844.3:c.5502G>A (ATM)	XP_011541146.1:p.Leu1834=
XM_011542845.2:c.5238G>A (ATM)	XP_011541147.1:p.Leu1746=
XM_017017789.2:c.6546G>A (ATM)	XP_016873278.1:p.Leu2182=
XM_017017790.2:c.6546G>A (ATM)	XP_016873279.1:p.Leu2182=
NM_001330368.2:c.641-12323C>T (C11orf65)	NP_001317297.1:n.641-12323C>T
NM_001351110.2:c.*39-12323C>T (C11orf65)	NP_001338039.1:n.*39-12323C>T
NM_001351834.2:c.6546G>A (ATM)	NP_001338763.1:p.Leu2182=
NM_000051.4:c.6546G>A (ATM) MANE Select	NP_000042.3:p.Leu2182=