Canonical Allele Identifier: CA394824653

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948222T>G , CM000678.2:g.13948222T>G	GRCh38
NC_000016.9:g.14042079T>G , CM000678.1:g.14042079T>G	GRCh37
NC_000016.8:g.13949580T>G	NCBI36
NG_011442.1:g.33066T>G , LRG_463:g.33066T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2626T>G MANE Select	NP_005227.1:p.Leu876Val
ENST00000311895.8:c.2626T>G MANE Select	ENSP00000310520.7:p.Leu876Val
NM_005236.2:c.2626T>G , LRG_463t1:c.2626T>G	NP_005227.1:p.Leu876Val
ENST00000311895.7:c.2626T>G	ENSP00000310520.7:p.Leu876Val
ENST00000389138.7:n.1903T>G
ENST00000682617.1:c.2764T>G	ENSP00000507912.1:p.Leu922Val
ENST00000683962.1:c.*2320T>G	ENSP00000506854.1:n.*2320T>G
XM_011522424.1:c.2764T>G	XP_011520726.1:p.Leu922Val
XM_011522424.3:c.2764T>G	XP_011520726.1:p.Leu922Val
XM_011522425.1:c.2083T>G	XP_011520727.1:p.Leu695Val
XM_011522426.1:c.1837T>G	XP_011520728.1:p.Leu613Val
XM_011522427.1:c.1276T>G	XP_011520729.1:p.Leu426Val
XM_017023043.2:c.1837T>G	XP_016878532.1:p.Leu613Val
XR_932805.1:n.2785T>G