Canonical Allele Identifier: CA812745159

Gene: ERCC8

Linked Data

• dbSNP Id: rs1331191809
• MyVariant Identifiers: chr5:g.60223669_60223672del (hg19) ; chr5:g.60927842_60927845del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60927845_60927848del , CM000667.2:g.60927845_60927848del	GRCh38
NC_000005.9:g.60223672_60223675del , CM000667.1:g.60223672_60223675del	GRCh37
NC_000005.8:g.60259429_60259432del	NCBI36
NG_009289.1:g.22234_22237del , LRG_466:g.22234_22237del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.173+1019_173+1022del	ENSP00000408344.2:n.173+1019_173+1022del
ENST00000647431.2:c.173+1019_173+1022del	ENSP00000494726.2:n.173+1019_173+1022del
ENST00000647486.2:c.173+1019_173+1022del	ENSP00000494466.2:n.173+1019_173+1022del
ENST00000675042.2:c.-2+1019_-2+1022del	ENSP00000502082.2:n.-2+1019_-2+1022del
ENST00000675452.2:c.173+1019_173+1022del	ENSP00000506954.1:n.173+1019_173+1022del
ENST00000682041.1:n.1242_1245del
ENST00000682217.1:c.173+1019_173+1022del	ENSP00000507570.1:n.173+1019_173+1022del
ENST00000682246.1:n.229+1019_229+1022del
ENST00000682375.1:c.-2+1019_-2+1022del	ENSP00000507551.1:n.-2+1019_-2+1022del
ENST00000682380.1:n.229+1019_229+1022del
ENST00000682418.1:n.229+1019_229+1022del
ENST00000682874.1:n.266_269del
ENST00000683052.1:c.78-9457_78-9454del	ENSP00000507072.1:n.78-9457_78-9454del
ENST00000683199.1:n.195+1019_195+1022del
ENST00000683460.1:c.173+1019_173+1022del	ENSP00000507820.1:n.173+1019_173+1022del
ENST00000684394.1:n.228+1019_228+1022del
ENST00000684453.1:n.223+1019_223+1022del
ENST00000684621.1:n.229+1019_229+1022del
ENST00000265038.10:c.173+1019_173+1022del	ENSP00000265038.6:n.173+1019_173+1022del
ENST00000497892.6:c.173+1019_173+1022del	ENSP00000501805.1:n.173+1019_173+1022del
ENST00000643034.1:c.173+1019_173+1022del	ENSP00000496080.1:n.173+1019_173+1022del
ENST00000643708.1:c.173+1019_173+1022del	ENSP00000494199.1:n.173+1019_173+1022del
ENST00000647431.1:c.124+1019_124+1022del
ENST00000647486.1:c.124+1019_124+1022del
ENST00000675042.1:c.-2+1019_-2+1022del	ENSP00000502082.1:n.-2+1019_-2+1022del
ENST00000675229.1:c.173+1019_173+1022del	ENSP00000502154.1:n.173+1019_173+1022del
ENST00000675378.1:c.173+1019_173+1022del	ENSP00000502535.1:n.173+1019_173+1022del
ENST00000675920.1:n.295-66_295-63del
ENST00000676185.1:c.173+1019_173+1022del MANE Select	ENSP00000501614.1:n.173+1019_173+1022del
ENST00000265038.9:c.173+1019_173+1022del	ENSP00000265038.5:n.173+1019_173+1022del
ENST00000381118.7:c.173+1019_173+1022del	ENSP00000370510.3:n.173+1019_173+1022del
ENST00000439176.5:c.-2+1019_-2+1022del	ENSP00000408344.1:n.-2+1019_-2+1022del
ENST00000477893.1:n.224+1019_224+1022del
ENST00000497892.5:n.216+1019_216+1022del
NM_000082.3:c.173+1019_173+1022del , LRG_466t1:c.173+1019_173+1022del	NP_000073.1:n.173+1019_173+1022del
NM_001007233.2:c.-220+1019_-220+1022del	NP_001007234.1:n.-220+1019_-220+1022del
NM_001007234.2:c.173+1019_173+1022del	NP_001007235.1:n.173+1019_173+1022del
NM_001290285.1:c.-205+1019_-205+1022del	NP_001277214.1:n.-205+1019_-205+1022del
NM_001007234.3:c.173+1019_173+1022del	NP_001007235.1:n.173+1019_173+1022del
NM_000082.4:c.173+1019_173+1022del MANE Select	NP_000073.1:n.173+1019_173+1022del
NM_001007233.3:c.-220+1019_-220+1022del	NP_001007234.1:n.-220+1019_-220+1022del
NM_001290285.2:c.-205+1019_-205+1022del	NP_001277214.1:n.-205+1019_-205+1022del