Canonical Allele Identifier: CA2209082779
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947915T= , CM000678.2:g.13947915T= GRCh38
NC_000016.9:g.14041772T= , CM000678.1:g.14041772T= GRCh37
NC_000016.8:g.13949273T= NCBI36
NG_011442.1:g.32759T= , LRG_463:g.32759T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2457T= ENSP00000507912.1:p.Gly819=
ENST00000683962.1:c.*2013T= ENSP00000506854.1:n.*2013T=
ENST00000311895.8:c.2319T= MANE Select ENSP00000310520.7:p.Gly773=
ENST00000311895.7:c.2319T= ENSP00000310520.7:p.Gly773=
ENST00000389138.7:n.1596T=
ENST00000462862.1:c.632T= ENSP00000461322.1:n.632T=
NM_005236.2:c.2319T= , LRG_463t1:c.2319T= NP_005227.1:p.Gly773=
XM_011522424.1:c.2457T= XP_011520726.1:p.Gly819=
XM_011522425.1:c.1776T= XP_011520727.1:p.Gly592=
XM_011522426.1:c.1530T= XP_011520728.1:p.Gly510=
XM_011522427.1:c.969T= XP_011520729.1:p.Gly323=
XR_932805.1:n.2478T=
XM_011522424.3:c.2457T= XP_011520726.1:p.Gly819=
XM_017023043.2:c.1530T= XP_016878532.1:p.Gly510=
NM_005236.3:c.2319T= MANE Select NP_005227.1:p.Gly773=