Canonical Allele Identifier: CA394823642
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948017T>A , CM000678.2:g.13948017T>A GRCh38
NC_000016.9:g.14041874T>A , CM000678.1:g.14041874T>A GRCh37
NC_000016.8:g.13949375T>A NCBI36
NG_011442.1:g.32861T>A , LRG_463:g.32861T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2559T>A ENSP00000507912.1:p.His853Gln
ENST00000683962.1:c.*2115T>A ENSP00000506854.1:n.*2115T>A
ENST00000311895.8:c.2421T>A MANE Select ENSP00000310520.7:p.His807Gln
ENST00000311895.7:c.2421T>A ENSP00000310520.7:p.His807Gln
ENST00000389138.7:n.1698T>A
NM_005236.2:c.2421T>A , LRG_463t1:c.2421T>A NP_005227.1:p.His807Gln
XM_011522424.1:c.2559T>A XP_011520726.1:p.His853Gln
XM_011522425.1:c.1878T>A XP_011520727.1:p.His626Gln
XM_011522426.1:c.1632T>A XP_011520728.1:p.His544Gln
XM_011522427.1:c.1071T>A XP_011520729.1:p.His357Gln
XR_932805.1:n.2580T>A
XM_011522424.3:c.2559T>A XP_011520726.1:p.His853Gln
XM_017023043.2:c.1632T>A XP_016878532.1:p.His544Gln
NM_005236.3:c.2421T>A MANE Select NP_005227.1:p.His807Gln