Canonical Allele Identifier: CA2209082884

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948145_13948148delinsACTT , CM000678.2:g.13948145_13948148delinsACTT	GRCh38
NC_000016.9:g.14042002_14042005delinsACTT , CM000678.1:g.14042002_14042005delinsACTT	GRCh37
NC_000016.8:g.13949503_13949506delinsACTT	NCBI36
NG_011442.1:g.32989_32992delinsACTT , LRG_463:g.32989_32992delinsACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2687_2690delinsACTT	ENSP00000507912.1:p.Asp896=
ENST00000683962.1:c.*2243_*2246delinsACTT	ENSP00000506854.1:n.*2243_*2246delinsACTT
ENST00000311895.8:c.2549_2552delinsACTT MANE Select	ENSP00000310520.7:p.Asp850=
ENST00000311895.7:c.2549_2552delinsACTT	ENSP00000310520.7:p.Asp850=
ENST00000389138.7:n.1826_1829delinsACTT
NM_005236.2:c.2549_2552delinsACTT , LRG_463t1:c.2549_2552delinsACTT	NP_005227.1:p.Asp850=
XM_011522424.1:c.2687_2690delinsACTT	XP_011520726.1:p.Asp896=
XM_011522425.1:c.2006_2009delinsACTT	XP_011520727.1:p.Asp669=
XM_011522426.1:c.1760_1763delinsACTT	XP_011520728.1:p.Asp587=
XM_011522427.1:c.1199_1202delinsACTT	XP_011520729.1:p.Asp400=
XR_932805.1:n.2708_2711delinsACTT
XM_011522424.3:c.2687_2690delinsACTT	XP_011520726.1:p.Asp896=
XM_017023043.2:c.1760_1763delinsACTT	XP_016878532.1:p.Asp587=
NM_005236.3:c.2549_2552delinsACTT MANE Select	NP_005227.1:p.Asp850=