Canonical Allele Identifier: CA1549989039

Gene: ERCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904683_60904685delinsTAA , CM000667.2:g.60904683_60904685delinsTAA	GRCh38
NC_000005.9:g.60200510_60200512delinsTAA , CM000667.1:g.60200510_60200512delinsTAA	GRCh37
NC_000005.8:g.60236267_60236269delinsTAA	NCBI36
NG_009289.1:g.45394_45396delinsTTA , LRG_466:g.45394_45396delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+107_481+109delinsTTA	ENSP00000408344.2:n.481+107_481+109delinsTTA
ENST00000647431.2:c.582+107_582+109delinsTTA	ENSP00000494726.2:n.582+107_582+109delinsTTA
ENST00000647486.2:c.481+107_481+109delinsTTA	ENSP00000494466.2:n.481+107_481+109delinsTTA
ENST00000675042.2:c.307+107_307+109delinsTTA	ENSP00000502082.2:n.307+107_307+109delinsTTA
ENST00000675452.2:c.*446+107_*446+109delinsTTA	ENSP00000506954.1:n.*446+107_*446+109delinsTTA
ENST00000682217.1:c.481+107_481+109delinsTTA	ENSP00000507570.1:n.481+107_481+109delinsTTA
ENST00000682246.1:n.537+107_537+109delinsTTA
ENST00000682375.1:c.*311+107_*311+109delinsTTA	ENSP00000507551.1:n.*311+107_*311+109delinsTTA
ENST00000683052.1:c.283+107_283+109delinsTTA	ENSP00000507072.1:n.283+107_283+109delinsTTA
ENST00000683199.1:n.503+107_503+109delinsTTA
ENST00000683216.1:n.750+103_750+105delinsTTA
ENST00000683460.1:c.*311+107_*311+109delinsTTA	ENSP00000507820.1:n.*311+107_*311+109delinsTTA
ENST00000684394.1:n.536+107_536+109delinsTTA
ENST00000684453.1:n.531+107_531+109delinsTTA
ENST00000684621.1:n.537+107_537+109delinsTTA
ENST00000265038.10:c.481+107_481+109delinsTTA	ENSP00000265038.6:n.481+107_481+109delinsTTA
ENST00000497892.6:c.*279+107_*279+109delinsTTA	ENSP00000501805.1:n.*279+107_*279+109delinsTTA
ENST00000643034.1:c.*373+107_*373+109delinsTTA	ENSP00000496080.1:n.*373+107_*373+109delinsTTA
ENST00000643708.1:c.*311+107_*311+109delinsTTA	ENSP00000494199.1:n.*311+107_*311+109delinsTTA
ENST00000647431.1:c.533+107_533+109delinsTTA
ENST00000647486.1:c.432+107_432+109delinsTTA
ENST00000675042.1:c.307+107_307+109delinsTTA	ENSP00000502082.1:n.307+107_307+109delinsTTA
ENST00000675229.1:c.481+107_481+109delinsTTA	ENSP00000502154.1:n.481+107_481+109delinsTTA
ENST00000675378.1:c.481+107_481+109delinsTTA	ENSP00000502535.1:n.481+107_481+109delinsTTA
ENST00000675452.1:n.730+107_730+109delinsTTA
ENST00000675920.1:n.1089+107_1089+109delinsTTA
ENST00000676185.1:c.481+107_481+109delinsTTA MANE Select	ENSP00000501614.1:n.481+107_481+109delinsTTA
ENST00000265038.9:c.481+107_481+109delinsTTA	ENSP00000265038.5:n.481+107_481+109delinsTTA
ENST00000381118.7:c.*525+107_*525+109delinsTTA	ENSP00000370510.3:n.*525+107_*525+109delinsTTA
ENST00000439176.5:c.307+107_307+109delinsTTA	ENSP00000408344.1:n.307+107_307+109delinsTTA
ENST00000462279.5:n.326+107_326+109delinsTTA
ENST00000484330.5:n.227-2177_227-2175delinsTTA
ENST00000495985.5:n.258+103_258+105delinsTTA
ENST00000497892.5:n.524+107_524+109delinsTTA
NM_000082.3:c.481+107_481+109delinsTTA , LRG_466t1:c.481+107_481+109delinsTTA	NP_000073.1:n.481+107_481+109delinsTTA
NM_001007233.2:c.307+107_307+109delinsTTA	NP_001007234.1:n.307+107_307+109delinsTTA
NM_001007234.2:c.481+107_481+109delinsTTA	NP_001007235.1:n.481+107_481+109delinsTTA
NM_001290285.1:c.23-969_23-967delinsTTA	NP_001277214.1:n.23-969_23-967delinsTTA
NM_001007234.3:c.481+107_481+109delinsTTA	NP_001007235.1:n.481+107_481+109delinsTTA
NM_000082.4:c.481+107_481+109delinsTTA MANE Select	NP_000073.1:n.481+107_481+109delinsTTA
NM_001007233.3:c.307+107_307+109delinsTTA	NP_001007234.1:n.307+107_307+109delinsTTA
NM_001290285.2:c.23-969_23-967delinsTTA	NP_001277214.1:n.23-969_23-967delinsTTA