Canonical Allele Identifier: CA2209082759
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947886_13947887delinsAG , CM000678.2:g.13947886_13947887delinsAG GRCh38
NC_000016.9:g.14041743_14041744delinsAG , CM000678.1:g.14041743_14041744delinsAG GRCh37
NC_000016.8:g.13949244_13949245delinsAG NCBI36
NG_011442.1:g.32730_32731delinsAG , LRG_463:g.32730_32731delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2428_2429delinsAG ENSP00000507912.1:p.Ser810=
ENST00000683962.1:c.*1984_*1985delinsAG ENSP00000506854.1:n.*1984_*1985delinsAG
ENST00000311895.8:c.2290_2291delinsAG MANE Select ENSP00000310520.7:p.Ser764=
ENST00000311895.7:c.2290_2291delinsAG ENSP00000310520.7:p.Ser764=
ENST00000389138.7:n.1567_1568delinsAG
ENST00000462862.1:c.603_604delinsAG ENSP00000461322.1:n.603_604delinsAG
NM_005236.2:c.2290_2291delinsAG , LRG_463t1:c.2290_2291delinsAG NP_005227.1:p.Ser764=
XM_011522424.1:c.2428_2429delinsAG XP_011520726.1:p.Ser810=
XM_011522425.1:c.1747_1748delinsAG XP_011520727.1:p.Ser583=
XM_011522426.1:c.1501_1502delinsAG XP_011520728.1:p.Ser501=
XM_011522427.1:c.940_941delinsAG XP_011520729.1:p.Ser314=
XR_932805.1:n.2449_2450delinsAG
XM_011522424.3:c.2428_2429delinsAG XP_011520726.1:p.Ser810=
XM_017023043.2:c.1501_1502delinsAG XP_016878532.1:p.Ser501=
NM_005236.3:c.2290_2291delinsAG MANE Select NP_005227.1:p.Ser764=