Canonical Allele Identifier: CA286972

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 127439
• ClinVar RCV Id: RCV001345281
• dbSNP Id: rs148949644
• MyVariant Identifiers: chr11:g.108199932G>T (hg19) ; chr11:g.108329205G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108329205G>T , CM000673.2:g.108329205G>T	GRCh38
NC_000011.9:g.108199932G>T , CM000673.1:g.108199932G>T	GRCh37
NC_000011.8:g.107705142G>T	NCBI36
NG_009830.1:g.111374G>T , LRG_135:g.111374G>T
NG_054724.1:g.145628C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.7274G>T (ATM)	ENSP00000388058.2:p.Gly2425Val
ENST00000713593.1:c.*6745G>T (ATM)	ENSP00000518889.1:n.*6745G>T
ENST00000278616.9:c.7274G>T (ATM)	ENSP00000278616.4:p.Gly2425Val
ENST00000525056.2:n.1693G>T (ATM)
ENST00000525537.3:n.231G>T (ATM)
ENST00000638786.2:n.111G>T (ATM)
ENST00000682286.1:n.2031G>T (ATM)
ENST00000682302.1:n.1692G>T (ATM)
ENST00000683174.1:n.8758G>T (ATM)
ENST00000683524.1:n.2498G>T (ATM)
ENST00000684152.1:n.2988G>T (ATM)
ENST00000684447.1:n.1737G>T (ATM)
ENST00000527805.6:c.*2338G>T (ATM)	ENSP00000435747.2:n.*2338G>T
ENST00000675595.1:c.*2409G>T (ATM)	ENSP00000502563.1:n.*2409G>T
ENST00000675843.1:c.7274G>T (ATM) MANE Select	ENSP00000501606.1:p.Gly2425Val
ENST00000278616.8:c.7274G>T (ATM)	ENSP00000278616.4:p.Gly2425Val
ENST00000452508.6:c.7274G>T (ATM)	ENSP00000388058.2:p.Gly2425Val
ENST00000524792.5:n.3489G>T (ATM)
ENST00000525537.2:n.550G>T (ATM)
ENST00000525729.5:c.641-20134C>A (C11orf65)	ENSP00000433395.1:n.641-20134C>A
ENST00000527389.2:n.299G>T (ATM)
ENST00000533690.5:n.2678G>T (ATM)
NM_000051.3:c.7274G>T , LRG_135t1:c.7274G>T (ATM)	NP_000042.3:p.Gly2425Val
XM_005271561.3:c.7274G>T (ATM)	XP_005271618.2:p.Gly2425Val
XM_005271562.3:c.7274G>T (ATM)	XP_005271619.2:p.Gly2425Val
XM_006718843.2:c.7274G>T (ATM)	XP_006718906.1:p.Gly2425Val
XM_006718845.1:c.3230G>T (ATM)	XP_006718908.1:p.Gly1077Val
XM_011542840.1:c.7274G>T (ATM)	XP_011541142.1:p.Gly2425Val
XM_011542841.1:c.7274G>T (ATM)	XP_011541143.1:p.Gly2425Val
XM_011542842.1:c.7109G>T (ATM)	XP_011541144.1:p.Gly2370Val
XM_011542843.1:c.7274G>T (ATM)	XP_011541145.1:p.Gly2425Val
XM_011542844.1:c.6230G>T (ATM)	XP_011541146.1:p.Gly2077Val
XM_011542845.1:c.5966G>T (ATM)	XP_011541147.1:p.Gly1989Val
XM_011542847.1:c.2345G>T (ATM)	XP_011541149.1:p.Gly782Val
NM_001330368.1:c.641-20134C>A (C11orf65)	NP_001317297.1:n.641-20134C>A
NM_001351110.1:c.*38+6015C>A (C11orf65)	NP_001338039.1:n.*38+6015C>A
NM_001351834.1:c.7274G>T (ATM)	NP_001338763.1:p.Gly2425Val
XM_005271562.5:c.7274G>T (ATM)	XP_005271619.2:p.Gly2425Val
XM_006718843.4:c.7274G>T (ATM)	XP_006718906.1:p.Gly2425Val
XM_006718845.2:c.3230G>T (ATM)	XP_006718908.1:p.Gly1077Val
XM_011542840.3:c.7274G>T (ATM)	XP_011541142.1:p.Gly2425Val
XM_011542842.3:c.7109G>T (ATM)	XP_011541144.1:p.Gly2370Val
XM_011542843.2:c.7274G>T (ATM)	XP_011541145.1:p.Gly2425Val
XM_011542844.3:c.6230G>T (ATM)	XP_011541146.1:p.Gly2077Val
XM_011542845.2:c.5966G>T (ATM)	XP_011541147.1:p.Gly1989Val
XM_017017789.2:c.7274G>T (ATM)	XP_016873278.1:p.Gly2425Val
XM_017017790.2:c.7274G>T (ATM)	XP_016873279.1:p.Gly2425Val
NM_001330368.2:c.641-20134C>A (C11orf65)	NP_001317297.1:n.641-20134C>A
NM_001351110.2:c.*38+6015C>A (C11orf65)	NP_001338039.1:n.*38+6015C>A
NM_001351834.2:c.7274G>T (ATM)	NP_001338763.1:p.Gly2425Val
NM_000051.4:c.7274G>T (ATM) MANE Select	NP_000042.3:p.Gly2425Val