Canonical Allele Identifier: CA2209082901
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948183T= , CM000678.2:g.13948183T= GRCh38
NC_000016.9:g.14042040T= , CM000678.1:g.14042040T= GRCh37
NC_000016.8:g.13949541T= NCBI36
NG_011442.1:g.33027T= , LRG_463:g.33027T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2725T= ENSP00000507912.1:p.Cys909=
ENST00000683962.1:c.*2281T= ENSP00000506854.1:n.*2281T=
ENST00000311895.8:c.2587T= MANE Select ENSP00000310520.7:p.Cys863=
ENST00000311895.7:c.2587T= ENSP00000310520.7:p.Cys863=
ENST00000389138.7:n.1864T=
NM_005236.2:c.2587T= , LRG_463t1:c.2587T= NP_005227.1:p.Cys863=
XM_011522424.1:c.2725T= XP_011520726.1:p.Cys909=
XM_011522425.1:c.2044T= XP_011520727.1:p.Cys682=
XM_011522426.1:c.1798T= XP_011520728.1:p.Cys600=
XM_011522427.1:c.1237T= XP_011520729.1:p.Cys413=
XR_932805.1:n.2746T=
XM_011522424.3:c.2725T= XP_011520726.1:p.Cys909=
XM_017023043.2:c.1798T= XP_016878532.1:p.Cys600=
NM_005236.3:c.2587T= MANE Select NP_005227.1:p.Cys863=