Canonical Allele Identifier: CA493689628

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947688C>T , CM000678.2:g.13947688C>T	GRCh38
NC_000016.9:g.14041545C>T , CM000678.1:g.14041545C>T	GRCh37
NC_000016.8:g.13949046C>T	NCBI36
NG_011442.1:g.32532C>T , LRG_463:g.32532C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2092C>T MANE Select	NP_005227.1:p.Leu698=
ENST00000311895.8:c.2092C>T MANE Select	ENSP00000310520.7:p.Leu698=
NM_005236.2:c.2092C>T , LRG_463t1:c.2092C>T	NP_005227.1:p.Leu698=
ENST00000311895.7:c.2092C>T	ENSP00000310520.7:p.Leu698=
ENST00000389138.7:n.1369C>T
ENST00000462862.1:c.405C>T	ENSP00000461322.1:n.405C>T
ENST00000682617.1:c.2230C>T	ENSP00000507912.1:p.Leu744=
ENST00000683962.1:c.*1786C>T	ENSP00000506854.1:n.*1786C>T
XM_011522424.1:c.2230C>T	XP_011520726.1:p.Leu744=
XM_011522424.3:c.2230C>T	XP_011520726.1:p.Leu744=
XM_011522425.1:c.1549C>T	XP_011520727.1:p.Leu517=
XM_011522426.1:c.1303C>T	XP_011520728.1:p.Leu435=
XM_011522427.1:c.742C>T	XP_011520729.1:p.Leu248=
XM_017023043.2:c.1303C>T	XP_016878532.1:p.Leu435=
XR_932805.1:n.2251C>T