Canonical Allele Identifier: CA2209082761

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947889A= , CM000678.2:g.13947889A=	GRCh38
NC_000016.9:g.14041746A= , CM000678.1:g.14041746A=	GRCh37
NC_000016.8:g.13949247A=	NCBI36
NG_011442.1:g.32733A= , LRG_463:g.32733A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2431A=	ENSP00000507912.1:p.Lys811=
ENST00000683962.1:c.*1987A=	ENSP00000506854.1:n.*1987A=
ENST00000311895.8:c.2293A= MANE Select	ENSP00000310520.7:p.Lys765=
ENST00000311895.7:c.2293A=	ENSP00000310520.7:p.Lys765=
ENST00000389138.7:n.1570A=
ENST00000462862.1:c.606A=	ENSP00000461322.1:n.606A=
NM_005236.2:c.2293A= , LRG_463t1:c.2293A=	NP_005227.1:p.Lys765=
XM_011522424.1:c.2431A=	XP_011520726.1:p.Lys811=
XM_011522425.1:c.1750A=	XP_011520727.1:p.Lys584=
XM_011522426.1:c.1504A=	XP_011520728.1:p.Lys502=
XM_011522427.1:c.943A=	XP_011520729.1:p.Lys315=
XR_932805.1:n.2452A=
XM_011522424.3:c.2431A=	XP_011520726.1:p.Lys811=
XM_017023043.2:c.1504A=	XP_016878532.1:p.Lys502=
NM_005236.3:c.2293A= MANE Select	NP_005227.1:p.Lys765=