Canonical Allele Identifier: CA359822317

Gene: ERCC8

Linked Data

• MyVariant Identifiers: chr5:g.60183275C>A (hg19) ; chr5:g.60887448C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60887448C>A , CM000667.2:g.60887448C>A	GRCh38
NC_000005.9:g.60183275C>A , CM000667.1:g.60183275C>A	GRCh37
NC_000005.8:g.60219032C>A	NCBI36
NG_009289.1:g.62631G>T , LRG_466:g.62631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.855+10828G>T	ENSP00000408344.2:n.855+10828G>T
ENST00000647431.2:c.1215G>T	ENSP00000494726.2:n.1215G>T
ENST00000675042.2:c.940G>T	ENSP00000502082.2:p.Asp314Tyr
ENST00000675452.2:c.*1079G>T	ENSP00000506954.1:n.*1079G>T
ENST00000682217.1:c.916G>T	ENSP00000507570.1:p.Asp306Tyr
ENST00000682375.1:c.*944G>T	ENSP00000507551.1:n.*944G>T
ENST00000683052.1:c.916G>T	ENSP00000507072.1:p.Asp306Tyr
ENST00000683216.1:n.4751G>T
ENST00000683460.1:c.*2551G>T	ENSP00000507820.1:n.*2551G>T
ENST00000683688.1:n.2860G>T
ENST00000684621.1:n.972G>T
ENST00000265038.10:c.1171G>T	ENSP00000265038.6:p.Asp391Tyr
ENST00000643034.1:c.*1006G>T	ENSP00000496080.1:n.*1006G>T
ENST00000643708.1:c.*944G>T	ENSP00000494199.1:n.*944G>T
ENST00000647431.1:c.1166G>T
ENST00000675378.1:c.*115G>T	ENSP00000502535.1:n.*115G>T
ENST00000675452.1:n.1363G>T
ENST00000676185.1:c.1114G>T MANE Select	ENSP00000501614.1:p.Asp372Tyr
ENST00000265038.9:c.1114G>T	ENSP00000265038.5:p.Asp372Tyr
ENST00000381118.7:c.*1158G>T	ENSP00000370510.3:n.*1158G>T
ENST00000462279.5:n.2566G>T
NM_000082.3:c.1114G>T , LRG_466t1:c.1114G>T	NP_000073.1:p.Asp372Tyr
NM_001007233.2:c.940G>T	NP_001007234.1:p.Asp314Tyr
NM_001290285.1:c.655G>T	NP_001277214.1:p.Asp219Tyr
NM_000082.4:c.1114G>T MANE Select	NP_000073.1:p.Asp372Tyr
NM_001007233.3:c.940G>T	NP_001007234.1:p.Asp314Tyr
NM_001290285.2:c.655G>T	NP_001277214.1:p.Asp219Tyr