Canonical Allele Identifier: CA2209081439
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13944813T= , CM000678.2:g.13944813T= GRCh38
NC_000016.9:g.14038670T= , CM000678.1:g.14038670T= GRCh37
NC_000016.8:g.13946171T= NCBI36
NG_011442.1:g.29657T= , LRG_463:g.29657T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2133T= ENSP00000507912.1:p.Val711=
ENST00000683962.1:c.*1689T= ENSP00000506854.1:n.*1689T=
ENST00000311895.8:c.1995T= MANE Select ENSP00000310520.7:p.Val665=
ENST00000311895.7:c.1995T= ENSP00000310520.7:p.Val665=
ENST00000389138.7:n.1272T=
ENST00000462862.1:c.308T= ENSP00000461322.1:n.308T=
NM_005236.2:c.1995T= , LRG_463t1:c.1995T= NP_005227.1:p.Val665=
XM_011522424.1:c.2133T= XP_011520726.1:p.Val711=
XM_011522425.1:c.1452T= XP_011520727.1:p.Val484=
XM_011522426.1:c.1206T= XP_011520728.1:p.Val402=
XM_011522427.1:c.645T= XP_011520729.1:p.Val215=
XR_932805.1:n.2154T=
XM_011522424.3:c.2133T= XP_011520726.1:p.Val711=
XM_017023043.2:c.1206T= XP_016878532.1:p.Val402=
NM_005236.3:c.1995T= MANE Select NP_005227.1:p.Val665=