Canonical Allele Identifier: CA559820765

Gene: ERCC8

Linked Data

• dbSNP Id: rs1274525891
• gnomAD v2: 5-60200473-A-ATATT
• gnomAD v3: 5-60904646-A-ATATT
• gnomAD v4: 5-60904646-A-ATATT
• MyVariant Identifiers: chr5:g.60200473_60200474insTATT (hg19) ; chr5:g.60904646_60904647insTATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904649_60904650insTTAT , CM000667.2:g.60904649_60904650insTTAT	GRCh38
NC_000005.9:g.60200476_60200477insTTAT , CM000667.1:g.60200476_60200477insTTAT	GRCh37
NC_000005.8:g.60236233_60236234insTTAT	NCBI36
NG_009289.1:g.45432_45433insAATA , LRG_466:g.45432_45433insAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+145_481+146insAATA	ENSP00000408344.2:n.481+145_481+146insAATA
ENST00000647431.2:c.582+145_582+146insAATA	ENSP00000494726.2:n.582+145_582+146insAATA
ENST00000647486.2:c.481+145_481+146insAATA	ENSP00000494466.2:n.481+145_481+146insAATA
ENST00000675042.2:c.307+145_307+146insAATA	ENSP00000502082.2:n.307+145_307+146insAATA
ENST00000675452.2:c.*446+145_*446+146insAATA	ENSP00000506954.1:n.*446+145_*446+146insAATA
ENST00000682217.1:c.481+145_481+146insAATA	ENSP00000507570.1:n.481+145_481+146insAATA
ENST00000682246.1:n.537+145_537+146insAATA
ENST00000682375.1:c.*311+145_*311+146insAATA	ENSP00000507551.1:n.*311+145_*311+146insAATA
ENST00000683052.1:c.283+145_283+146insAATA	ENSP00000507072.1:n.283+145_283+146insAATA
ENST00000683199.1:n.503+145_503+146insAATA
ENST00000683216.1:n.750+141_750+142insAATA
ENST00000683460.1:c.*311+145_*311+146insAATA	ENSP00000507820.1:n.*311+145_*311+146insAATA
ENST00000684394.1:n.536+145_536+146insAATA
ENST00000684453.1:n.531+145_531+146insAATA
ENST00000684621.1:n.537+145_537+146insAATA
ENST00000265038.10:c.481+145_481+146insAATA	ENSP00000265038.6:n.481+145_481+146insAATA
ENST00000497892.6:c.*279+145_*279+146insAATA	ENSP00000501805.1:n.*279+145_*279+146insAATA
ENST00000643034.1:c.*373+145_*373+146insAATA	ENSP00000496080.1:n.*373+145_*373+146insAATA
ENST00000643708.1:c.*311+145_*311+146insAATA	ENSP00000494199.1:n.*311+145_*311+146insAATA
ENST00000647431.1:c.533+145_533+146insAATA
ENST00000647486.1:c.432+145_432+146insAATA
ENST00000675042.1:c.307+145_307+146insAATA	ENSP00000502082.1:n.307+145_307+146insAATA
ENST00000675229.1:c.481+145_481+146insAATA	ENSP00000502154.1:n.481+145_481+146insAATA
ENST00000675378.1:c.481+145_481+146insAATA	ENSP00000502535.1:n.481+145_481+146insAATA
ENST00000675452.1:n.730+145_730+146insAATA
ENST00000675920.1:n.1089+145_1089+146insAATA
ENST00000676185.1:c.481+145_481+146insAATA MANE Select	ENSP00000501614.1:n.481+145_481+146insAATA
ENST00000265038.9:c.481+145_481+146insAATA	ENSP00000265038.5:n.481+145_481+146insAATA
ENST00000381118.7:c.*525+145_*525+146insAATA	ENSP00000370510.3:n.*525+145_*525+146insAATA
ENST00000439176.5:c.307+145_307+146insAATA	ENSP00000408344.1:n.307+145_307+146insAATA
ENST00000462279.5:n.326+145_326+146insAATA
ENST00000484330.5:n.227-2139_227-2138insAATA
ENST00000495985.5:n.258+141_258+142insAATA
ENST00000497892.5:n.524+145_524+146insAATA
NM_000082.3:c.481+145_481+146insAATA , LRG_466t1:c.481+145_481+146insAATA	NP_000073.1:n.481+145_481+146insAATA
NM_001007233.2:c.307+145_307+146insAATA	NP_001007234.1:n.307+145_307+146insAATA
NM_001007234.2:c.481+145_481+146insAATA	NP_001007235.1:n.481+145_481+146insAATA
NM_001290285.1:c.23-931_23-930insAATA	NP_001277214.1:n.23-931_23-930insAATA
NM_001007234.3:c.481+145_481+146insAATA	NP_001007235.1:n.481+145_481+146insAATA
NM_000082.4:c.481+145_481+146insAATA MANE Select	NP_000073.1:n.481+145_481+146insAATA
NM_001007233.3:c.307+145_307+146insAATA	NP_001007234.1:n.307+145_307+146insAATA
NM_001290285.2:c.23-931_23-930insAATA	NP_001277214.1:n.23-931_23-930insAATA