Canonical Allele Identifier: CA2209082785
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947927G= , CM000678.2:g.13947927G= GRCh38
NC_000016.9:g.14041784G= , CM000678.1:g.14041784G= GRCh37
NC_000016.8:g.13949285G= NCBI36
NG_011442.1:g.32771G= , LRG_463:g.32771G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2469G= ENSP00000507912.1:p.Gln823=
ENST00000683962.1:c.*2025G= ENSP00000506854.1:n.*2025G=
ENST00000311895.8:c.2331G= MANE Select ENSP00000310520.7:p.Gln777=
ENST00000311895.7:c.2331G= ENSP00000310520.7:p.Gln777=
ENST00000389138.7:n.1608G=
ENST00000462862.1:c.644G= ENSP00000461322.1:n.644G=
NM_005236.2:c.2331G= , LRG_463t1:c.2331G= NP_005227.1:p.Gln777=
XM_011522424.1:c.2469G= XP_011520726.1:p.Gln823=
XM_011522425.1:c.1788G= XP_011520727.1:p.Gln596=
XM_011522426.1:c.1542G= XP_011520728.1:p.Gln514=
XM_011522427.1:c.981G= XP_011520729.1:p.Gln327=
XR_932805.1:n.2490G=
XM_011522424.3:c.2469G= XP_011520726.1:p.Gln823=
XM_017023043.2:c.1542G= XP_016878532.1:p.Gln514=
NM_005236.3:c.2331G= MANE Select NP_005227.1:p.Gln777=