Canonical Allele Identifier: CA394821774

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141619850
• MyVariant Identifiers: chr16:g.14041560G>A (hg19) ; chr16:g.13947703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947703G>A , CM000678.2:g.13947703G>A	GRCh38
NC_000016.9:g.14041560G>A , CM000678.1:g.14041560G>A	GRCh37
NC_000016.8:g.13949061G>A	NCBI36
NG_011442.1:g.32547G>A , LRG_463:g.32547G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2245G>A	ENSP00000507912.1:p.Gly749Ser
ENST00000683962.1:c.*1801G>A	ENSP00000506854.1:n.*1801G>A
ENST00000311895.8:c.2107G>A MANE Select	ENSP00000310520.7:p.Gly703Ser
ENST00000311895.7:c.2107G>A	ENSP00000310520.7:p.Gly703Ser
ENST00000389138.7:n.1384G>A
ENST00000462862.1:c.420G>A	ENSP00000461322.1:n.420G>A
NM_005236.2:c.2107G>A , LRG_463t1:c.2107G>A	NP_005227.1:p.Gly703Ser
XM_011522424.1:c.2245G>A	XP_011520726.1:p.Gly749Ser
XM_011522425.1:c.1564G>A	XP_011520727.1:p.Gly522Ser
XM_011522426.1:c.1318G>A	XP_011520728.1:p.Gly440Ser
XM_011522427.1:c.757G>A	XP_011520729.1:p.Gly253Ser
XR_932805.1:n.2266G>A
XM_011522424.3:c.2245G>A	XP_011520726.1:p.Gly749Ser
XM_017023043.2:c.1318G>A	XP_016878532.1:p.Gly440Ser
NM_005236.3:c.2107G>A MANE Select	NP_005227.1:p.Gly703Ser