Canonical Allele Identifier: CA2209082794
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947954C= , CM000678.2:g.13947954C= GRCh38
NC_000016.9:g.14041811C= , CM000678.1:g.14041811C= GRCh37
NC_000016.8:g.13949312C= NCBI36
NG_011442.1:g.32798C= , LRG_463:g.32798C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2496C= ENSP00000507912.1:p.Ser832=
ENST00000683962.1:c.*2052C= ENSP00000506854.1:n.*2052C=
ENST00000311895.8:c.2358C= MANE Select ENSP00000310520.7:p.Ser786=
ENST00000311895.7:c.2358C= ENSP00000310520.7:p.Ser786=
ENST00000389138.7:n.1635C=
ENST00000462862.1:c.671C= ENSP00000461322.1:n.671C=
NM_005236.2:c.2358C= , LRG_463t1:c.2358C= NP_005227.1:p.Ser786=
XM_011522424.1:c.2496C= XP_011520726.1:p.Ser832=
XM_011522425.1:c.1815C= XP_011520727.1:p.Ser605=
XM_011522426.1:c.1569C= XP_011520728.1:p.Ser523=
XM_011522427.1:c.1008C= XP_011520729.1:p.Ser336=
XR_932805.1:n.2517C=
XM_011522424.3:c.2496C= XP_011520726.1:p.Ser832=
XM_017023043.2:c.1569C= XP_016878532.1:p.Ser523=
NM_005236.3:c.2358C= MANE Select NP_005227.1:p.Ser786=