Canonical Allele Identifier: CA2209082753

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947881_13947882delinsAC , CM000678.2:g.13947881_13947882delinsAC	GRCh38
NC_000016.9:g.14041738_14041739delinsAC , CM000678.1:g.14041738_14041739delinsAC	GRCh37
NC_000016.8:g.13949239_13949240delinsAC	NCBI36
NG_011442.1:g.32725_32726delinsAC , LRG_463:g.32725_32726delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2423_2424delinsAC	ENSP00000507912.1:p.Asp808=
ENST00000683962.1:c.*1979_*1980delinsAC	ENSP00000506854.1:n.*1979_*1980delinsAC
ENST00000311895.8:c.2285_2286delinsAC MANE Select	ENSP00000310520.7:p.Asp762=
ENST00000311895.7:c.2285_2286delinsAC	ENSP00000310520.7:p.Asp762=
ENST00000389138.7:n.1562_1563delinsAC
ENST00000462862.1:c.598_599delinsAC	ENSP00000461322.1:n.598_599delinsAC
NM_005236.2:c.2285_2286delinsAC , LRG_463t1:c.2285_2286delinsAC	NP_005227.1:p.Asp762=
XM_011522424.1:c.2423_2424delinsAC	XP_011520726.1:p.Asp808=
XM_011522425.1:c.1742_1743delinsAC	XP_011520727.1:p.Asp581=
XM_011522426.1:c.1496_1497delinsAC	XP_011520728.1:p.Asp499=
XM_011522427.1:c.935_936delinsAC	XP_011520729.1:p.Asp312=
XR_932805.1:n.2444_2445delinsAC
XM_011522424.3:c.2423_2424delinsAC	XP_011520726.1:p.Asp808=
XM_017023043.2:c.1496_1497delinsAC	XP_016878532.1:p.Asp499=
NM_005236.3:c.2285_2286delinsAC MANE Select	NP_005227.1:p.Asp762=