Canonical Allele Identifier: CA1549989031

Gene: ERCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904678_60904683delinsATATAT , CM000667.2:g.60904678_60904683delinsATATAT	GRCh38
NC_000005.9:g.60200505_60200510delinsATATAT , CM000667.1:g.60200505_60200510delinsATATAT	GRCh37
NC_000005.8:g.60236262_60236267delinsATATAT	NCBI36
NG_009289.1:g.45396_45401delinsATATAT , LRG_466:g.45396_45401delinsATATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+109_481+114delinsATATAT	ENSP00000408344.2:n.481+109_481+114delinsATATAT
ENST00000647431.2:c.582+109_582+114delinsATATAT	ENSP00000494726.2:n.582+109_582+114delinsATATAT
ENST00000647486.2:c.481+109_481+114delinsATATAT	ENSP00000494466.2:n.481+109_481+114delinsATATAT
ENST00000675042.2:c.307+109_307+114delinsATATAT	ENSP00000502082.2:n.307+109_307+114delinsATATAT
ENST00000675452.2:c.*446+109_*446+114delinsATATAT	ENSP00000506954.1:n.*446+109_*446+114delinsATATAT
ENST00000682217.1:c.481+109_481+114delinsATATAT	ENSP00000507570.1:n.481+109_481+114delinsATATAT
ENST00000682246.1:n.537+109_537+114delinsATATAT
ENST00000682375.1:c.*311+109_*311+114delinsATATAT	ENSP00000507551.1:n.*311+109_*311+114delinsATATAT
ENST00000683052.1:c.283+109_283+114delinsATATAT	ENSP00000507072.1:n.283+109_283+114delinsATATAT
ENST00000683199.1:n.503+109_503+114delinsATATAT
ENST00000683216.1:n.750+105_750+110delinsATATAT
ENST00000683460.1:c.*311+109_*311+114delinsATATAT	ENSP00000507820.1:n.*311+109_*311+114delinsATATAT
ENST00000684394.1:n.536+109_536+114delinsATATAT
ENST00000684453.1:n.531+109_531+114delinsATATAT
ENST00000684621.1:n.537+109_537+114delinsATATAT
ENST00000265038.10:c.481+109_481+114delinsATATAT	ENSP00000265038.6:n.481+109_481+114delinsATATAT
ENST00000497892.6:c.*279+109_*279+114delinsATATAT	ENSP00000501805.1:n.*279+109_*279+114delinsATATAT
ENST00000643034.1:c.*373+109_*373+114delinsATATAT	ENSP00000496080.1:n.*373+109_*373+114delinsATATAT
ENST00000643708.1:c.*311+109_*311+114delinsATATAT	ENSP00000494199.1:n.*311+109_*311+114delinsATATAT
ENST00000647431.1:c.533+109_533+114delinsATATAT
ENST00000647486.1:c.432+109_432+114delinsATATAT
ENST00000675042.1:c.307+109_307+114delinsATATAT	ENSP00000502082.1:n.307+109_307+114delinsATATAT
ENST00000675229.1:c.481+109_481+114delinsATATAT	ENSP00000502154.1:n.481+109_481+114delinsATATAT
ENST00000675378.1:c.481+109_481+114delinsATATAT	ENSP00000502535.1:n.481+109_481+114delinsATATAT
ENST00000675452.1:n.730+109_730+114delinsATATAT
ENST00000675920.1:n.1089+109_1089+114delinsATATAT
ENST00000676185.1:c.481+109_481+114delinsATATAT MANE Select	ENSP00000501614.1:n.481+109_481+114delinsATATAT
ENST00000265038.9:c.481+109_481+114delinsATATAT	ENSP00000265038.5:n.481+109_481+114delinsATATAT
ENST00000381118.7:c.*525+109_*525+114delinsATATAT	ENSP00000370510.3:n.*525+109_*525+114delinsATATAT
ENST00000439176.5:c.307+109_307+114delinsATATAT	ENSP00000408344.1:n.307+109_307+114delinsATATAT
ENST00000462279.5:n.326+109_326+114delinsATATAT
ENST00000484330.5:n.227-2175_227-2170delinsATATAT
ENST00000495985.5:n.258+105_258+110delinsATATAT
ENST00000497892.5:n.524+109_524+114delinsATATAT
NM_000082.3:c.481+109_481+114delinsATATAT , LRG_466t1:c.481+109_481+114delinsATATAT	NP_000073.1:n.481+109_481+114delinsATATAT
NM_001007233.2:c.307+109_307+114delinsATATAT	NP_001007234.1:n.307+109_307+114delinsATATAT
NM_001007234.2:c.481+109_481+114delinsATATAT	NP_001007235.1:n.481+109_481+114delinsATATAT
NM_001290285.1:c.23-967_23-962delinsATATAT	NP_001277214.1:n.23-967_23-962delinsATATAT
NM_001007234.3:c.481+109_481+114delinsATATAT	NP_001007235.1:n.481+109_481+114delinsATATAT
NM_000082.4:c.481+109_481+114delinsATATAT MANE Select	NP_000073.1:n.481+109_481+114delinsATATAT
NM_001007233.3:c.307+109_307+114delinsATATAT	NP_001007234.1:n.307+109_307+114delinsATATAT
NM_001290285.2:c.23-967_23-962delinsATATAT	NP_001277214.1:n.23-967_23-962delinsATATAT