Canonical Allele Identifier: CA382559380

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 479043
• ClinVar RCV Id: RCV000569192 ; RCV000820773
• dbSNP Id: rs1555121919
• MyVariant Identifiers: chr11:g.108199749C>T (hg19) ; chr11:g.108329022C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108329022C>T , CM000673.2:g.108329022C>T	GRCh38
NC_000011.9:g.108199749C>T , CM000673.1:g.108199749C>T	GRCh37
NC_000011.8:g.107704959C>T	NCBI36
NG_009830.1:g.111191C>T , LRG_135:g.111191C>T
NG_054724.1:g.145811G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.7091C>T (ATM)	ENSP00000388058.2:p.Ala2364Val
ENST00000713593.1:c.*6562C>T (ATM)	ENSP00000518889.1:n.*6562C>T
ENST00000278616.9:c.7091C>T (ATM)	ENSP00000278616.4:p.Ala2364Val
ENST00000525056.2:n.1510C>T (ATM)
ENST00000525537.3:n.48C>T (ATM)
ENST00000682286.1:n.1848C>T (ATM)
ENST00000682302.1:n.1509C>T (ATM)
ENST00000683174.1:n.8575C>T (ATM)
ENST00000683524.1:n.2315C>T (ATM)
ENST00000684152.1:n.2805C>T (ATM)
ENST00000684447.1:n.1554C>T (ATM)
ENST00000527805.6:c.*2155C>T (ATM)	ENSP00000435747.2:n.*2155C>T
ENST00000675595.1:c.*2226C>T (ATM)	ENSP00000502563.1:n.*2226C>T
ENST00000675843.1:c.7091C>T (ATM) MANE Select	ENSP00000501606.1:p.Ala2364Val
ENST00000278616.8:c.7091C>T (ATM)	ENSP00000278616.4:p.Ala2364Val
ENST00000452508.6:c.7091C>T (ATM)	ENSP00000388058.2:p.Ala2364Val
ENST00000524792.5:n.3306C>T (ATM)
ENST00000525537.2:n.367C>T (ATM)
ENST00000525729.5:c.641-19951G>A (C11orf65)	ENSP00000433395.1:n.641-19951G>A
ENST00000527389.2:n.116C>T (ATM)
ENST00000533690.5:n.2495C>T (ATM)
NM_000051.3:c.7091C>T , LRG_135t1:c.7091C>T (ATM)	NP_000042.3:p.Ala2364Val
XM_005271561.3:c.7091C>T (ATM)	XP_005271618.2:p.Ala2364Val
XM_005271562.3:c.7091C>T (ATM)	XP_005271619.2:p.Ala2364Val
XM_006718843.2:c.7091C>T (ATM)	XP_006718906.1:p.Ala2364Val
XM_006718845.1:c.3047C>T (ATM)	XP_006718908.1:p.Ala1016Val
XM_011542840.1:c.7091C>T (ATM)	XP_011541142.1:p.Ala2364Val
XM_011542841.1:c.7091C>T (ATM)	XP_011541143.1:p.Ala2364Val
XM_011542842.1:c.6926C>T (ATM)	XP_011541144.1:p.Ala2309Val
XM_011542843.1:c.7091C>T (ATM)	XP_011541145.1:p.Ala2364Val
XM_011542844.1:c.6047C>T (ATM)	XP_011541146.1:p.Ala2016Val
XM_011542845.1:c.5783C>T (ATM)	XP_011541147.1:p.Ala1928Val
XM_011542847.1:c.2162C>T (ATM)	XP_011541149.1:p.Ala721Val
NM_001330368.1:c.641-19951G>A (C11orf65)	NP_001317297.1:n.641-19951G>A
NM_001351110.1:c.*38+6198G>A (C11orf65)	NP_001338039.1:n.*38+6198G>A
NM_001351834.1:c.7091C>T (ATM)	NP_001338763.1:p.Ala2364Val
XM_005271562.5:c.7091C>T (ATM)	XP_005271619.2:p.Ala2364Val
XM_006718843.4:c.7091C>T (ATM)	XP_006718906.1:p.Ala2364Val
XM_006718845.2:c.3047C>T (ATM)	XP_006718908.1:p.Ala1016Val
XM_011542840.3:c.7091C>T (ATM)	XP_011541142.1:p.Ala2364Val
XM_011542842.3:c.6926C>T (ATM)	XP_011541144.1:p.Ala2309Val
XM_011542843.2:c.7091C>T (ATM)	XP_011541145.1:p.Ala2364Val
XM_011542844.3:c.6047C>T (ATM)	XP_011541146.1:p.Ala2016Val
XM_011542845.2:c.5783C>T (ATM)	XP_011541147.1:p.Ala1928Val
XM_017017789.2:c.7091C>T (ATM)	XP_016873278.1:p.Ala2364Val
XM_017017790.2:c.7091C>T (ATM)	XP_016873279.1:p.Ala2364Val
NM_001330368.2:c.641-19951G>A (C11orf65)	NP_001317297.1:n.641-19951G>A
NM_001351110.2:c.*38+6198G>A (C11orf65)	NP_001338039.1:n.*38+6198G>A
NM_001351834.2:c.7091C>T (ATM)	NP_001338763.1:p.Ala2364Val
NM_000051.4:c.7091C>T (ATM) MANE Select	NP_000042.3:p.Ala2364Val