Canonical Allele Identifier: CA2209082877
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948135G= , CM000678.2:g.13948135G= GRCh38
NC_000016.9:g.14041992G= , CM000678.1:g.14041992G= GRCh37
NC_000016.8:g.13949493G= NCBI36
NG_011442.1:g.32979G= , LRG_463:g.32979G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2677G= ENSP00000507912.1:p.Gly893=
ENST00000683962.1:c.*2233G= ENSP00000506854.1:n.*2233G=
ENST00000311895.8:c.2539G= MANE Select ENSP00000310520.7:p.Gly847=
ENST00000311895.7:c.2539G= ENSP00000310520.7:p.Gly847=
ENST00000389138.7:n.1816G=
NM_005236.2:c.2539G= , LRG_463t1:c.2539G= NP_005227.1:p.Gly847=
XM_011522424.1:c.2677G= XP_011520726.1:p.Gly893=
XM_011522425.1:c.1996G= XP_011520727.1:p.Gly666=
XM_011522426.1:c.1750G= XP_011520728.1:p.Gly584=
XM_011522427.1:c.1189G= XP_011520729.1:p.Gly397=
XR_932805.1:n.2698G=
XM_011522424.3:c.2677G= XP_011520726.1:p.Gly893=
XM_017023043.2:c.1750G= XP_016878532.1:p.Gly584=
NM_005236.3:c.2539G= MANE Select NP_005227.1:p.Gly847=