Canonical Allele Identifier: CA2209082828
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948021A= , CM000678.2:g.13948021A= GRCh38
NC_000016.9:g.14041878A= , CM000678.1:g.14041878A= GRCh37
NC_000016.8:g.13949379A= NCBI36
NG_011442.1:g.32865A= , LRG_463:g.32865A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2563A= ENSP00000507912.1:p.Thr855=
ENST00000683962.1:c.*2119A= ENSP00000506854.1:n.*2119A=
ENST00000311895.8:c.2425A= MANE Select ENSP00000310520.7:p.Thr809=
ENST00000311895.7:c.2425A= ENSP00000310520.7:p.Thr809=
ENST00000389138.7:n.1702A=
NM_005236.2:c.2425A= , LRG_463t1:c.2425A= NP_005227.1:p.Thr809=
XM_011522424.1:c.2563A= XP_011520726.1:p.Thr855=
XM_011522425.1:c.1882A= XP_011520727.1:p.Thr628=
XM_011522426.1:c.1636A= XP_011520728.1:p.Thr546=
XM_011522427.1:c.1075A= XP_011520729.1:p.Thr359=
XR_932805.1:n.2584A=
XM_011522424.3:c.2563A= XP_011520726.1:p.Thr855=
XM_017023043.2:c.1636A= XP_016878532.1:p.Thr546=
NM_005236.3:c.2425A= MANE Select NP_005227.1:p.Thr809=