Canonical Allele Identifier: CA913188403

Gene: ATM C11orf65

Linked Data

• ClinVar Variation Id: 846024
• ClinVar RCV Id: RCV001049218
• dbSNP Id: rs2085083193

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108320009_108320010del , CM000673.2:g.108320009_108320010del	GRCh38
NC_000011.9:g.108190736_108190737del , CM000673.1:g.108190736_108190737del	GRCh37
NC_000011.8:g.107695946_107695947del	NCBI36
NG_009830.1:g.102178_102179del , LRG_135:g.102178_102179del
NG_054724.1:g.154826_154827del

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.6403_6404del (ATM)	ENSP00000388058.2:p.Leu2135LysfsTer10
ENST00000713593.1:c.*5874_*5875del (ATM)	ENSP00000518889.1:n.*5874_*5875del
ENST00000278616.9:c.6403_6404del (ATM)	ENSP00000278616.4:p.Leu2135LysfsTer10
ENST00000525056.2:n.822_823del (ATM)
ENST00000682286.1:n.1160_1161del (ATM)
ENST00000682302.1:n.821_822del (ATM)
ENST00000683174.1:n.7887_7888del (ATM)
ENST00000683524.1:n.1627_1628del (ATM)
ENST00000684152.1:n.2117_2118del (ATM)
ENST00000527805.6:c.*1467_*1468del (ATM)	ENSP00000435747.2:n.*1467_*1468del
ENST00000675595.1:c.*1467_*1468del (ATM)	ENSP00000502563.1:n.*1467_*1468del
ENST00000675843.1:c.6403_6404del (ATM) MANE Select	ENSP00000501606.1:p.Leu2135LysfsTer10
ENST00000278616.8:c.6403_6404del (ATM)	ENSP00000278616.4:p.Leu2135LysfsTer10
ENST00000452508.6:c.6403_6404del (ATM)	ENSP00000388058.2:p.Leu2135LysfsTer10
ENST00000524792.5:n.2618_2619del (ATM)
ENST00000525729.5:c.641-10936_641-10935del (C11orf65)	ENSP00000433395.1:n.641-10936_641-10935de...
ENST00000533690.5:n.1807_1808del (ATM)
NM_000051.3:c.6403_6404del , LRG_135t1:c.6403_6404del (ATM)	NP_000042.3:p.Leu2135LysfsTer10
XM_005271561.3:c.6403_6404del (ATM)	XP_005271618.2:p.Leu2135LysfsTer10
XM_005271562.3:c.6403_6404del (ATM)	XP_005271619.2:p.Leu2135LysfsTer10
XM_006718843.2:c.6403_6404del (ATM)	XP_006718906.1:p.Leu2135LysfsTer10
XM_006718845.1:c.2359_2360del (ATM)	XP_006718908.1:p.Leu787LysfsTer10
XM_011542840.1:c.6403_6404del (ATM)	XP_011541142.1:p.Leu2135LysfsTer10
XM_011542841.1:c.6403_6404del (ATM)	XP_011541143.1:p.Leu2135LysfsTer10
XM_011542842.1:c.6238_6239del (ATM)	XP_011541144.1:p.Leu2080LysfsTer10
XM_011542843.1:c.6403_6404del (ATM)	XP_011541145.1:p.Leu2135LysfsTer10
XM_011542844.1:c.5359_5360del (ATM)	XP_011541146.1:p.Leu1787LysfsTer10
XM_011542845.1:c.5095_5096del (ATM)	XP_011541147.1:p.Leu1699LysfsTer10
XM_011542847.1:c.1474_1475del (ATM)	XP_011541149.1:p.Leu492LysfsTer10
NM_001330368.1:c.641-10936_641-10935del (C11orf65)	NP_001317297.1:n.641-10936_641-10935del
NM_001351110.1:c.*39-10936_*39-10935del (C11orf65)	NP_001338039.1:n.*39-10936_*39-10935del
NM_001351834.1:c.6403_6404del (ATM)	NP_001338763.1:p.Leu2135LysfsTer10
XM_005271562.5:c.6403_6404del (ATM)	XP_005271619.2:p.Leu2135LysfsTer10
XM_006718843.4:c.6403_6404del (ATM)	XP_006718906.1:p.Leu2135LysfsTer10
XM_006718845.2:c.2359_2360del (ATM)	XP_006718908.1:p.Leu787LysfsTer10
XM_011542840.3:c.6403_6404del (ATM)	XP_011541142.1:p.Leu2135LysfsTer10
XM_011542842.3:c.6238_6239del (ATM)	XP_011541144.1:p.Leu2080LysfsTer10
XM_011542843.2:c.6403_6404del (ATM)	XP_011541145.1:p.Leu2135LysfsTer10
XM_011542844.3:c.5359_5360del (ATM)	XP_011541146.1:p.Leu1787LysfsTer10
XM_011542845.2:c.5095_5096del (ATM)	XP_011541147.1:p.Leu1699LysfsTer10
XM_017017789.2:c.6403_6404del (ATM)	XP_016873278.1:p.Leu2135LysfsTer10
XM_017017790.2:c.6403_6404del (ATM)	XP_016873279.1:p.Leu2135LysfsTer10
XM_017017791.1:c.6403_6404del (ATM)	XP_016873280.1:p.Leu2135LysfsTer10
NM_001330368.2:c.641-10936_641-10935del (C11orf65)	NP_001317297.1:n.641-10936_641-10935del
NM_001351110.2:c.*39-10936_*39-10935del (C11orf65)	NP_001338039.1:n.*39-10936_*39-10935del
NM_001351834.2:c.6403_6404del (ATM)	NP_001338763.1:p.Leu2135LysfsTer10
NM_000051.4:c.6403_6404del (ATM) MANE Select	NP_000042.3:p.Leu2135LysfsTer10