Canonical Allele Identifier: CA394821590

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947682C>A , CM000678.2:g.13947682C>A	GRCh38
NC_000016.9:g.14041539C>A , CM000678.1:g.14041539C>A	GRCh37
NC_000016.8:g.13949040C>A	NCBI36
NG_011442.1:g.32526C>A , LRG_463:g.32526C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2086C>A MANE Select	NP_005227.1:p.Pro696Thr
ENST00000311895.8:c.2086C>A MANE Select	ENSP00000310520.7:p.Pro696Thr
NM_005236.2:c.2086C>A , LRG_463t1:c.2086C>A	NP_005227.1:p.Pro696Thr
ENST00000311895.7:c.2086C>A	ENSP00000310520.7:p.Pro696Thr
ENST00000389138.7:n.1363C>A
ENST00000462862.1:c.399C>A	ENSP00000461322.1:n.399C>A
ENST00000682617.1:c.2224C>A	ENSP00000507912.1:p.Pro742Thr
ENST00000683962.1:c.*1780C>A	ENSP00000506854.1:n.*1780C>A
XM_011522424.1:c.2224C>A	XP_011520726.1:p.Pro742Thr
XM_011522424.3:c.2224C>A	XP_011520726.1:p.Pro742Thr
XM_011522425.1:c.1543C>A	XP_011520727.1:p.Pro515Thr
XM_011522426.1:c.1297C>A	XP_011520728.1:p.Pro433Thr
XM_011522427.1:c.736C>A	XP_011520729.1:p.Pro246Thr
XM_017023043.2:c.1297C>A	XP_016878532.1:p.Pro433Thr
XR_932805.1:n.2245C>A