Canonical Allele Identifier: CA2209082652

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947661C= , CM000678.2:g.13947661C=	GRCh38
NC_000016.9:g.14041518C= , CM000678.1:g.14041518C=	GRCh37
NC_000016.8:g.13949019C=	NCBI36
NG_011442.1:g.32505C= , LRG_463:g.32505C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2203C=	ENSP00000507912.1:p.Arg735=
ENST00000683962.1:c.*1759C=	ENSP00000506854.1:n.*1759C=
ENST00000311895.8:c.2065C= MANE Select	ENSP00000310520.7:p.Arg689=
ENST00000311895.7:c.2065C=	ENSP00000310520.7:p.Arg689=
ENST00000389138.7:n.1342C=
ENST00000462862.1:c.378C=	ENSP00000461322.1:n.378C=
NM_005236.2:c.2065C= , LRG_463t1:c.2065C=	NP_005227.1:p.Arg689=
XM_011522424.1:c.2203C=	XP_011520726.1:p.Arg735=
XM_011522425.1:c.1522C=	XP_011520727.1:p.Arg508=
XM_011522426.1:c.1276C=	XP_011520728.1:p.Arg426=
XM_011522427.1:c.715C=	XP_011520729.1:p.Arg239=
XR_932805.1:n.2224C=
XM_011522424.3:c.2203C=	XP_011520726.1:p.Arg735=
XM_017023043.2:c.1276C=	XP_016878532.1:p.Arg426=
NM_005236.3:c.2065C= MANE Select	NP_005227.1:p.Arg689=