Canonical Allele Identifier: CA2209082937
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948246C= , CM000678.2:g.13948246C= GRCh38
NC_000016.9:g.14042103C= , CM000678.1:g.14042103C= GRCh37
NC_000016.8:g.13949604C= NCBI36
NG_011442.1:g.33090C= , LRG_463:g.33090C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2788C= ENSP00000507912.1:p.Leu930=
ENST00000683962.1:c.*2344C= ENSP00000506854.1:n.*2344C=
ENST00000311895.8:c.2650C= MANE Select ENSP00000310520.7:p.Leu884=
ENST00000311895.7:c.2650C= ENSP00000310520.7:p.Leu884=
ENST00000389138.7:n.1927C=
NM_005236.2:c.2650C= , LRG_463t1:c.2650C= NP_005227.1:p.Leu884=
XM_011522424.1:c.2788C= XP_011520726.1:p.Leu930=
XM_011522425.1:c.2107C= XP_011520727.1:p.Leu703=
XM_011522426.1:c.1861C= XP_011520728.1:p.Leu621=
XM_011522427.1:c.1300C= XP_011520729.1:p.Leu434=
XR_932805.1:n.2809C=
XM_011522424.3:c.2788C= XP_011520726.1:p.Leu930=
XM_017023043.2:c.1861C= XP_016878532.1:p.Leu621=
NM_005236.3:c.2650C= MANE Select NP_005227.1:p.Leu884=