Canonical Allele Identifier: CA2831377721

Gene: ERCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904639_60904640insCT , CM000667.2:g.60904639_60904640insCT	GRCh38
NC_000005.9:g.60200466_60200467insCT , CM000667.1:g.60200466_60200467insCT	GRCh37
NC_000005.8:g.60236223_60236224insCT	NCBI36
NG_009289.1:g.45440_45441insGA , LRG_466:g.45440_45441insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+153_481+154insGA	ENSP00000408344.2:n.481+153_481+154insGA
ENST00000647431.2:c.582+153_582+154insGA	ENSP00000494726.2:n.582+153_582+154insGA
ENST00000647486.2:c.481+153_481+154insGA	ENSP00000494466.2:n.481+153_481+154insGA
ENST00000675042.2:c.307+153_307+154insGA	ENSP00000502082.2:n.307+153_307+154insGA
ENST00000675452.2:c.*446+153_*446+154insGA	ENSP00000506954.1:n.*446+153_*446+154insGA
ENST00000682217.1:c.481+153_481+154insGA	ENSP00000507570.1:n.481+153_481+154insGA
ENST00000682246.1:n.537+153_537+154insGA
ENST00000682375.1:c.*311+153_*311+154insGA	ENSP00000507551.1:n.*311+153_*311+154insGA
ENST00000683052.1:c.283+153_283+154insGA	ENSP00000507072.1:n.283+153_283+154insGA
ENST00000683199.1:n.503+153_503+154insGA
ENST00000683216.1:n.750+149_750+150insGA
ENST00000683460.1:c.*311+153_*311+154insGA	ENSP00000507820.1:n.*311+153_*311+154insGA
ENST00000684394.1:n.536+153_536+154insGA
ENST00000684453.1:n.531+153_531+154insGA
ENST00000684621.1:n.537+153_537+154insGA
ENST00000265038.10:c.481+153_481+154insGA	ENSP00000265038.6:n.481+153_481+154insGA
ENST00000497892.6:c.*279+153_*279+154insGA	ENSP00000501805.1:n.*279+153_*279+154insGA
ENST00000643034.1:c.*373+153_*373+154insGA	ENSP00000496080.1:n.*373+153_*373+154insGA
ENST00000643708.1:c.*311+153_*311+154insGA	ENSP00000494199.1:n.*311+153_*311+154insGA
ENST00000647431.1:c.533+153_533+154insGA
ENST00000647486.1:c.432+153_432+154insGA
ENST00000675042.1:c.307+153_307+154insGA	ENSP00000502082.1:n.307+153_307+154insGA
ENST00000675229.1:c.481+153_481+154insGA	ENSP00000502154.1:n.481+153_481+154insGA
ENST00000675378.1:c.481+153_481+154insGA	ENSP00000502535.1:n.481+153_481+154insGA
ENST00000675452.1:n.730+153_730+154insGA
ENST00000675920.1:n.1089+153_1089+154insGA
ENST00000676185.1:c.481+153_481+154insGA MANE Select	ENSP00000501614.1:n.481+153_481+154insGA
ENST00000265038.9:c.481+153_481+154insGA	ENSP00000265038.5:n.481+153_481+154insGA
ENST00000381118.7:c.*525+153_*525+154insGA	ENSP00000370510.3:n.*525+153_*525+154insGA
ENST00000439176.5:c.307+153_307+154insGA	ENSP00000408344.1:n.307+153_307+154insGA
ENST00000462279.5:n.326+153_326+154insGA
ENST00000484330.5:n.227-2131_227-2130insGA
ENST00000495985.5:n.258+149_258+150insGA
ENST00000497892.5:n.524+153_524+154insGA
NM_000082.3:c.481+153_481+154insGA , LRG_466t1:c.481+153_481+154insGA	NP_000073.1:n.481+153_481+154insGA
NM_001007233.2:c.307+153_307+154insGA	NP_001007234.1:n.307+153_307+154insGA
NM_001007234.2:c.481+153_481+154insGA	NP_001007235.1:n.481+153_481+154insGA
NM_001290285.1:c.23-923_23-922insGA	NP_001277214.1:n.23-923_23-922insGA
NM_001007234.3:c.481+153_481+154insGA	NP_001007235.1:n.481+153_481+154insGA
NM_000082.4:c.481+153_481+154insGA MANE Select	NP_000073.1:n.481+153_481+154insGA
NM_001007233.3:c.307+153_307+154insGA	NP_001007234.1:n.307+153_307+154insGA
NM_001290285.2:c.23-923_23-922insGA	NP_001277214.1:n.23-923_23-922insGA