Canonical Allele Identifier: CA559820743

Gene: ERCC8

Linked Data

• ClinVar Variation Id: 1205170
• ClinVar RCV Id: RCV001571750
• dbSNP Id: rs1387048989
• gnomAD v2: 5-60200455-GTGTGTGTATATA-G
• gnomAD v3: 5-60904628-GTGTGTGTATATA-G
• gnomAD v4: 5-60904628-GTGTGTGTATATA-G
• MyVariant Identifiers: chr5:g.60200456_60200467del (hg19) ; chr5:g.60200457_60200485delinsATATATATATATATATA (hg19) ; chr5:g.60904629_60904640del (hg38) ; chr5:g.60904630_60904658delinsATATATATATATATATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904630_60904641del , CM000667.2:g.60904630_60904641del	GRCh38
NC_000005.9:g.60200457_60200468del , CM000667.1:g.60200457_60200468del	GRCh37
NC_000005.8:g.60236214_60236225del	NCBI36
NG_009289.1:g.45439_45450del , LRG_466:g.45439_45450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+152_481+163del	ENSP00000408344.2:n.481+152_481+163del
ENST00000647431.2:c.582+152_582+163del	ENSP00000494726.2:n.582+152_582+163del
ENST00000647486.2:c.481+152_481+163del	ENSP00000494466.2:n.481+152_481+163del
ENST00000675042.2:c.307+152_307+163del	ENSP00000502082.2:n.307+152_307+163del
ENST00000675452.2:c.*446+152_*446+163del	ENSP00000506954.1:n.*446+152_*446+163del
ENST00000682217.1:c.481+152_481+163del	ENSP00000507570.1:n.481+152_481+163del
ENST00000682246.1:n.537+152_537+163del
ENST00000682375.1:c.*311+152_*311+163del	ENSP00000507551.1:n.*311+152_*311+163del
ENST00000683052.1:c.283+152_283+163del	ENSP00000507072.1:n.283+152_283+163del
ENST00000683199.1:n.503+152_503+163del
ENST00000683216.1:n.750+148_750+159del
ENST00000683460.1:c.*311+152_*311+163del	ENSP00000507820.1:n.*311+152_*311+163del
ENST00000684394.1:n.536+152_536+163del
ENST00000684453.1:n.531+152_531+163del
ENST00000684621.1:n.537+152_537+163del
ENST00000265038.10:c.481+152_481+163del	ENSP00000265038.6:n.481+152_481+163del
ENST00000497892.6:c.*279+152_*279+163del	ENSP00000501805.1:n.*279+152_*279+163del
ENST00000643034.1:c.*373+152_*373+163del	ENSP00000496080.1:n.*373+152_*373+163del
ENST00000643708.1:c.*311+152_*311+163del	ENSP00000494199.1:n.*311+152_*311+163del
ENST00000647431.1:c.533+152_533+163del
ENST00000647486.1:c.432+152_432+163del
ENST00000675042.1:c.307+152_307+163del	ENSP00000502082.1:n.307+152_307+163del
ENST00000675229.1:c.481+152_481+163del	ENSP00000502154.1:n.481+152_481+163del
ENST00000675378.1:c.481+152_481+163del	ENSP00000502535.1:n.481+152_481+163del
ENST00000675452.1:n.730+152_730+163del
ENST00000675920.1:n.1089+152_1089+163del
ENST00000676185.1:c.481+152_481+163del MANE Select	ENSP00000501614.1:n.481+152_481+163del
ENST00000265038.9:c.481+152_481+163del	ENSP00000265038.5:n.481+152_481+163del
ENST00000381118.7:c.*525+152_*525+163del	ENSP00000370510.3:n.*525+152_*525+163del
ENST00000439176.5:c.307+152_307+163del	ENSP00000408344.1:n.307+152_307+163del
ENST00000462279.5:n.326+152_326+163del
ENST00000484330.5:n.227-2132_227-2121del
ENST00000495985.5:n.258+148_258+159del
ENST00000497892.5:n.524+152_524+163del
NM_000082.3:c.481+152_481+163del , LRG_466t1:c.481+152_481+163del	NP_000073.1:n.481+152_481+163del
NM_001007233.2:c.307+152_307+163del	NP_001007234.1:n.307+152_307+163del
NM_001007234.2:c.481+152_481+163del	NP_001007235.1:n.481+152_481+163del
NM_001290285.1:c.23-924_23-913del	NP_001277214.1:n.23-924_23-913del
NM_001007234.3:c.481+152_481+163del	NP_001007235.1:n.481+152_481+163del
NM_000082.4:c.481+152_481+163del MANE Select	NP_000073.1:n.481+152_481+163del
NM_001007233.3:c.307+152_307+163del	NP_001007234.1:n.307+152_307+163del
NM_001290285.2:c.23-924_23-913del	NP_001277214.1:n.23-924_23-913del