Canonical Allele Identifier: CA2209081563

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13945072_13945073delinsAC , CM000678.2:g.13945072_13945073delinsAC	GRCh38
NC_000016.9:g.14038929_14038930delinsAC , CM000678.1:g.14038929_14038930delinsAC	GRCh37
NC_000016.8:g.13946430_13946431delinsAC	NCBI36
NG_011442.1:g.29916_29917delinsAC , LRG_463:g.29916_29917delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2155+237_2155+238delinsAC	ENSP00000507912.1:n.2155+237_2155+238delinsAC
ENST00000683962.1:c.*1711+237_*1711+238delinsAC	ENSP00000506854.1:n.*1711+237_*1711+238delinsAC
ENST00000311895.8:c.2017+237_2017+238delinsAC MANE Select	ENSP00000310520.7:n.2017+237_2017+238delinsAC
ENST00000311895.7:c.2017+237_2017+238delinsAC	ENSP00000310520.7:n.2017+237_2017+238delinsAC
ENST00000389138.7:n.1294+237_1294+238delinsAC
ENST00000462862.1:c.330+237_330+238delinsAC	ENSP00000461322.1:n.330+237_330+238delinsAC
NM_005236.2:c.2017+237_2017+238delinsAC , LRG_463t1:c.2017+237_2017+238delinsAC	NP_005227.1:n.2017+237_2017+238delinsAC
XM_011522424.1:c.2155+237_2155+238delinsAC	XP_011520726.1:n.2155+237_2155+238delinsAC
XM_011522425.1:c.1474+237_1474+238delinsAC	XP_011520727.1:n.1474+237_1474+238delinsAC
XM_011522426.1:c.1228+237_1228+238delinsAC	XP_011520728.1:n.1228+237_1228+238delinsAC
XM_011522427.1:c.667+237_667+238delinsAC	XP_011520729.1:n.667+237_667+238delinsAC
XR_932805.1:n.2176+237_2176+238delinsAC
XM_011522424.3:c.2155+237_2155+238delinsAC	XP_011520726.1:n.2155+237_2155+238delinsAC
XM_017023043.2:c.1228+237_1228+238delinsAC	XP_016878532.1:n.1228+237_1228+238delinsAC
NM_005236.3:c.2017+237_2017+238delinsAC MANE Select	NP_005227.1:n.2017+237_2017+238delinsAC