Canonical Allele Identifier: CA382556960

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 482550
• ClinVar RCV Id: RCV000563605 ; RCV000628105
• dbSNP Id: rs1060501668
• MyVariant Identifiers: chr11:g.108196878G>C (hg19) ; chr11:g.108326151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108326151G>C , CM000673.2:g.108326151G>C	GRCh38
NC_000011.9:g.108196878G>C , CM000673.1:g.108196878G>C	GRCh37
NC_000011.8:g.107702088G>C	NCBI36
NG_009830.1:g.108320G>C , LRG_135:g.108320G>C
NG_054724.1:g.148682C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6901G>C (ATM)	ENSP00000388058.2:p.Ala2301Pro
ENST00000713593.1:c.*6372G>C (ATM)	ENSP00000518889.1:n.*6372G>C
ENST00000278616.9:c.6901G>C (ATM)	ENSP00000278616.4:p.Ala2301Pro
ENST00000525056.2:n.1320G>C (ATM)
ENST00000682286.1:n.1658G>C (ATM)
ENST00000682302.1:n.1319G>C (ATM)
ENST00000683174.1:n.8385G>C (ATM)
ENST00000683524.1:n.2125G>C (ATM)
ENST00000684152.1:n.2615G>C (ATM)
ENST00000527805.6:c.*1965G>C (ATM)	ENSP00000435747.2:n.*1965G>C
ENST00000675595.1:c.*2036G>C (ATM)	ENSP00000502563.1:n.*2036G>C
ENST00000675843.1:c.6901G>C (ATM) MANE Select	ENSP00000501606.1:p.Ala2301Pro
ENST00000278616.8:c.6901G>C (ATM)	ENSP00000278616.4:p.Ala2301Pro
ENST00000452508.6:c.6901G>C (ATM)	ENSP00000388058.2:p.Ala2301Pro
ENST00000524792.5:n.3116G>C (ATM)
ENST00000525729.5:c.641-17080C>G (C11orf65)	ENSP00000433395.1:n.641-17080C>G
ENST00000533690.5:n.2305G>C (ATM)
NM_000051.3:c.6901G>C , LRG_135t1:c.6901G>C (ATM)	NP_000042.3:p.Ala2301Pro
XM_005271561.3:c.6901G>C (ATM)	XP_005271618.2:p.Ala2301Pro
XM_005271562.3:c.6901G>C (ATM)	XP_005271619.2:p.Ala2301Pro
XM_006718843.2:c.6901G>C (ATM)	XP_006718906.1:p.Ala2301Pro
XM_006718845.1:c.2857G>C (ATM)	XP_006718908.1:p.Ala953Pro
XM_011542840.1:c.6901G>C (ATM)	XP_011541142.1:p.Ala2301Pro
XM_011542841.1:c.6901G>C (ATM)	XP_011541143.1:p.Ala2301Pro
XM_011542842.1:c.6736G>C (ATM)	XP_011541144.1:p.Ala2246Pro
XM_011542843.1:c.6901G>C (ATM)	XP_011541145.1:p.Ala2301Pro
XM_011542844.1:c.5857G>C (ATM)	XP_011541146.1:p.Ala1953Pro
XM_011542845.1:c.5593G>C (ATM)	XP_011541147.1:p.Ala1865Pro
XM_011542847.1:c.1972G>C (ATM)	XP_011541149.1:p.Ala658Pro
NM_001330368.1:c.641-17080C>G (C11orf65)	NP_001317297.1:n.641-17080C>G
NM_001351110.1:c.*38+9069C>G (C11orf65)	NP_001338039.1:n.*38+9069C>G
NM_001351834.1:c.6901G>C (ATM)	NP_001338763.1:p.Ala2301Pro
XM_005271562.5:c.6901G>C (ATM)	XP_005271619.2:p.Ala2301Pro
XM_006718843.4:c.6901G>C (ATM)	XP_006718906.1:p.Ala2301Pro
XM_006718845.2:c.2857G>C (ATM)	XP_006718908.1:p.Ala953Pro
XM_011542840.3:c.6901G>C (ATM)	XP_011541142.1:p.Ala2301Pro
XM_011542842.3:c.6736G>C (ATM)	XP_011541144.1:p.Ala2246Pro
XM_011542843.2:c.6901G>C (ATM)	XP_011541145.1:p.Ala2301Pro
XM_011542844.3:c.5857G>C (ATM)	XP_011541146.1:p.Ala1953Pro
XM_011542845.2:c.5593G>C (ATM)	XP_011541147.1:p.Ala1865Pro
XM_017017789.2:c.6901G>C (ATM)	XP_016873278.1:p.Ala2301Pro
XM_017017790.2:c.6901G>C (ATM)	XP_016873279.1:p.Ala2301Pro
NM_001330368.2:c.641-17080C>G (C11orf65)	NP_001317297.1:n.641-17080C>G
NM_001351110.2:c.*38+9069C>G (C11orf65)	NP_001338039.1:n.*38+9069C>G
NM_001351834.2:c.6901G>C (ATM)	NP_001338763.1:p.Ala2301Pro
NM_000051.4:c.6901G>C (ATM) MANE Select	NP_000042.3:p.Ala2301Pro