Canonical Allele Identifier: CA2209082905
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948187G= , CM000678.2:g.13948187G= GRCh38
NC_000016.9:g.14042044G= , CM000678.1:g.14042044G= GRCh37
NC_000016.8:g.13949545G= NCBI36
NG_011442.1:g.33031G= , LRG_463:g.33031G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2729G= ENSP00000507912.1:p.Arg910=
ENST00000683962.1:c.*2285G= ENSP00000506854.1:n.*2285G=
ENST00000311895.8:c.2591G= MANE Select ENSP00000310520.7:p.Arg864=
ENST00000311895.7:c.2591G= ENSP00000310520.7:p.Arg864=
ENST00000389138.7:n.1868G=
NM_005236.2:c.2591G= , LRG_463t1:c.2591G= NP_005227.1:p.Arg864=
XM_011522424.1:c.2729G= XP_011520726.1:p.Arg910=
XM_011522425.1:c.2048G= XP_011520727.1:p.Arg683=
XM_011522426.1:c.1802G= XP_011520728.1:p.Arg601=
XM_011522427.1:c.1241G= XP_011520729.1:p.Arg414=
XR_932805.1:n.2750G=
XM_011522424.3:c.2729G= XP_011520726.1:p.Arg910=
XM_017023043.2:c.1802G= XP_016878532.1:p.Arg601=
NM_005236.3:c.2591G= MANE Select NP_005227.1:p.Arg864=