Canonical Allele Identifier: CA1549988991
Gene: ERCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60904663T= , CM000667.2:g.60904663T= GRCh38
NC_000005.9:g.60200490T= , CM000667.1:g.60200490T= GRCh37
NC_000005.8:g.60236247T= NCBI36
NG_009289.1:g.45416A= , LRG_466:g.45416A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439176.6:c.481+129A= ENSP00000408344.2:n.481+129A=
ENST00000647431.2:c.582+129A= ENSP00000494726.2:n.582+129A=
ENST00000647486.2:c.481+129A= ENSP00000494466.2:n.481+129A=
ENST00000675042.2:c.307+129A= ENSP00000502082.2:n.307+129A=
ENST00000675452.2:c.*446+129A= ENSP00000506954.1:n.*446+129A=
ENST00000682217.1:c.481+129A= ENSP00000507570.1:n.481+129A=
ENST00000682246.1:n.537+129A=
ENST00000682375.1:c.*311+129A= ENSP00000507551.1:n.*311+129A=
ENST00000683052.1:c.283+129A= ENSP00000507072.1:n.283+129A=
ENST00000683199.1:n.503+129A=
ENST00000683216.1:n.750+125A=
ENST00000683460.1:c.*311+129A= ENSP00000507820.1:n.*311+129A=
ENST00000684394.1:n.536+129A=
ENST00000684453.1:n.531+129A=
ENST00000684621.1:n.537+129A=
ENST00000265038.10:c.481+129A= ENSP00000265038.6:n.481+129A=
ENST00000497892.6:c.*279+129A= ENSP00000501805.1:n.*279+129A=
ENST00000643034.1:c.*373+129A= ENSP00000496080.1:n.*373+129A=
ENST00000643708.1:c.*311+129A= ENSP00000494199.1:n.*311+129A=
ENST00000647431.1:c.533+129A=
ENST00000647486.1:c.432+129A=
ENST00000675042.1:c.307+129A= ENSP00000502082.1:n.307+129A=
ENST00000675229.1:c.481+129A= ENSP00000502154.1:n.481+129A=
ENST00000675378.1:c.481+129A= ENSP00000502535.1:n.481+129A=
ENST00000675452.1:n.730+129A=
ENST00000675920.1:n.1089+129A=
ENST00000676185.1:c.481+129A= MANE Select ENSP00000501614.1:n.481+129A=
ENST00000265038.9:c.481+129A= ENSP00000265038.5:n.481+129A=
ENST00000381118.7:c.*525+129A= ENSP00000370510.3:n.*525+129A=
ENST00000439176.5:c.307+129A= ENSP00000408344.1:n.307+129A=
ENST00000462279.5:n.326+129A=
ENST00000484330.5:n.227-2155A=
ENST00000495985.5:n.258+125A=
ENST00000497892.5:n.524+129A=
NM_000082.3:c.481+129A= , LRG_466t1:c.481+129A= NP_000073.1:n.481+129A=
NM_001007233.2:c.307+129A= NP_001007234.1:n.307+129A=
NM_001007234.2:c.481+129A= NP_001007235.1:n.481+129A=
NM_001290285.1:c.23-947A= NP_001277214.1:n.23-947A=
NM_001007234.3:c.481+129A= NP_001007235.1:n.481+129A=
NM_000082.4:c.481+129A= MANE Select NP_000073.1:n.481+129A=
NM_001007233.3:c.307+129A= NP_001007234.1:n.307+129A=
NM_001290285.2:c.23-947A= NP_001277214.1:n.23-947A=