Canonical Allele Identifier: CA359822500

Gene: ERCC8

Linked Data

• MyVariant Identifiers: chr5:g.60183299A>C (hg19) ; chr5:g.60887472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60887472A>C , CM000667.2:g.60887472A>C	GRCh38
NC_000005.9:g.60183299A>C , CM000667.1:g.60183299A>C	GRCh37
NC_000005.8:g.60219056A>C	NCBI36
NG_009289.1:g.62607T>G , LRG_466:g.62607T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.855+10804T>G	ENSP00000408344.2:n.855+10804T>G
ENST00000647431.2:c.1191T>G	ENSP00000494726.2:n.1191T>G
ENST00000675042.2:c.916T>G	ENSP00000502082.2:p.Ser306Ala
ENST00000675452.2:c.*1055T>G	ENSP00000506954.1:n.*1055T>G
ENST00000682217.1:c.892T>G	ENSP00000507570.1:p.Ser298Ala
ENST00000682375.1:c.*920T>G	ENSP00000507551.1:n.*920T>G
ENST00000683052.1:c.892T>G	ENSP00000507072.1:p.Ser298Ala
ENST00000683216.1:n.4727T>G
ENST00000683460.1:c.*2527T>G	ENSP00000507820.1:n.*2527T>G
ENST00000683688.1:n.2836T>G
ENST00000684621.1:n.948T>G
ENST00000265038.10:c.1147T>G	ENSP00000265038.6:p.Ser383Ala
ENST00000643034.1:c.*982T>G	ENSP00000496080.1:n.*982T>G
ENST00000643708.1:c.*920T>G	ENSP00000494199.1:n.*920T>G
ENST00000647431.1:c.1142T>G
ENST00000675378.1:c.*91T>G	ENSP00000502535.1:n.*91T>G
ENST00000675452.1:n.1339T>G
ENST00000676185.1:c.1090T>G MANE Select	ENSP00000501614.1:p.Ser364Ala
ENST00000265038.9:c.1090T>G	ENSP00000265038.5:p.Ser364Ala
ENST00000381118.7:c.*1134T>G	ENSP00000370510.3:n.*1134T>G
ENST00000462279.5:n.2542T>G
NM_000082.3:c.1090T>G , LRG_466t1:c.1090T>G	NP_000073.1:p.Ser364Ala
NM_001007233.2:c.916T>G	NP_001007234.1:p.Ser306Ala
NM_001290285.1:c.631T>G	NP_001277214.1:p.Ser211Ala
NM_000082.4:c.1090T>G MANE Select	NP_000073.1:p.Ser364Ala
NM_001007233.3:c.916T>G	NP_001007234.1:p.Ser306Ala
NM_001290285.2:c.631T>G	NP_001277214.1:p.Ser211Ala