Canonical Allele Identifier: CA1549988949

Gene: ERCC8

Linked Data

• dbSNP Id: rs1749009359

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904637_60904638insGT , CM000667.2:g.60904637_60904638insGT	GRCh38
NC_000005.9:g.60200464_60200465insGT , CM000667.1:g.60200464_60200465insGT	GRCh37
NC_000005.8:g.60236221_60236222insGT	NCBI36
NG_009289.1:g.45442_45443insCA , LRG_466:g.45442_45443insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+155_481+156insCA	ENSP00000408344.2:n.481+155_481+156insCA
ENST00000647431.2:c.582+155_582+156insCA	ENSP00000494726.2:n.582+155_582+156insCA
ENST00000647486.2:c.481+155_481+156insCA	ENSP00000494466.2:n.481+155_481+156insCA
ENST00000675042.2:c.307+155_307+156insCA	ENSP00000502082.2:n.307+155_307+156insCA
ENST00000675452.2:c.*446+155_*446+156insCA	ENSP00000506954.1:n.*446+155_*446+156insCA
ENST00000682217.1:c.481+155_481+156insCA	ENSP00000507570.1:n.481+155_481+156insCA
ENST00000682246.1:n.537+155_537+156insCA
ENST00000682375.1:c.*311+155_*311+156insCA	ENSP00000507551.1:n.*311+155_*311+156insCA
ENST00000683052.1:c.283+155_283+156insCA	ENSP00000507072.1:n.283+155_283+156insCA
ENST00000683199.1:n.503+155_503+156insCA
ENST00000683216.1:n.750+151_750+152insCA
ENST00000683460.1:c.*311+155_*311+156insCA	ENSP00000507820.1:n.*311+155_*311+156insCA
ENST00000684394.1:n.536+155_536+156insCA
ENST00000684453.1:n.531+155_531+156insCA
ENST00000684621.1:n.537+155_537+156insCA
ENST00000265038.10:c.481+155_481+156insCA	ENSP00000265038.6:n.481+155_481+156insCA
ENST00000497892.6:c.*279+155_*279+156insCA	ENSP00000501805.1:n.*279+155_*279+156insCA
ENST00000643034.1:c.*373+155_*373+156insCA	ENSP00000496080.1:n.*373+155_*373+156insCA
ENST00000643708.1:c.*311+155_*311+156insCA	ENSP00000494199.1:n.*311+155_*311+156insCA
ENST00000647431.1:c.533+155_533+156insCA
ENST00000647486.1:c.432+155_432+156insCA
ENST00000675042.1:c.307+155_307+156insCA	ENSP00000502082.1:n.307+155_307+156insCA
ENST00000675229.1:c.481+155_481+156insCA	ENSP00000502154.1:n.481+155_481+156insCA
ENST00000675378.1:c.481+155_481+156insCA	ENSP00000502535.1:n.481+155_481+156insCA
ENST00000675452.1:n.730+155_730+156insCA
ENST00000675920.1:n.1089+155_1089+156insCA
ENST00000676185.1:c.481+155_481+156insCA MANE Select	ENSP00000501614.1:n.481+155_481+156insCA
ENST00000265038.9:c.481+155_481+156insCA	ENSP00000265038.5:n.481+155_481+156insCA
ENST00000381118.7:c.*525+155_*525+156insCA	ENSP00000370510.3:n.*525+155_*525+156insCA
ENST00000439176.5:c.307+155_307+156insCA	ENSP00000408344.1:n.307+155_307+156insCA
ENST00000462279.5:n.326+155_326+156insCA
ENST00000484330.5:n.227-2129_227-2128insCA
ENST00000495985.5:n.258+151_258+152insCA
ENST00000497892.5:n.524+155_524+156insCA
NM_000082.3:c.481+155_481+156insCA , LRG_466t1:c.481+155_481+156insCA	NP_000073.1:n.481+155_481+156insCA
NM_001007233.2:c.307+155_307+156insCA	NP_001007234.1:n.307+155_307+156insCA
NM_001007234.2:c.481+155_481+156insCA	NP_001007235.1:n.481+155_481+156insCA
NM_001290285.1:c.23-921_23-920insCA	NP_001277214.1:n.23-921_23-920insCA
NM_001007234.3:c.481+155_481+156insCA	NP_001007235.1:n.481+155_481+156insCA
NM_000082.4:c.481+155_481+156insCA MANE Select	NP_000073.1:n.481+155_481+156insCA
NM_001007233.3:c.307+155_307+156insCA	NP_001007234.1:n.307+155_307+156insCA
NM_001290285.2:c.23-921_23-920insCA	NP_001277214.1:n.23-921_23-920insCA