Canonical Allele Identifier: CA394818030

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038662G>A (hg19) ; chr16:g.13944805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944805G>A , CM000678.2:g.13944805G>A	GRCh38
NC_000016.9:g.14038662G>A , CM000678.1:g.14038662G>A	GRCh37
NC_000016.8:g.13946163G>A	NCBI36
NG_011442.1:g.29649G>A , LRG_463:g.29649G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2125G>A	ENSP00000507912.1:p.Ala709Thr
ENST00000683962.1:c.*1681G>A	ENSP00000506854.1:n.*1681G>A
ENST00000311895.8:c.1987G>A MANE Select	ENSP00000310520.7:p.Ala663Thr
ENST00000311895.7:c.1987G>A	ENSP00000310520.7:p.Ala663Thr
ENST00000389138.7:n.1264G>A
ENST00000462862.1:c.300G>A	ENSP00000461322.1:n.300G>A
NM_005236.2:c.1987G>A , LRG_463t1:c.1987G>A	NP_005227.1:p.Ala663Thr
XM_011522424.1:c.2125G>A	XP_011520726.1:p.Ala709Thr
XM_011522425.1:c.1444G>A	XP_011520727.1:p.Ala482Thr
XM_011522426.1:c.1198G>A	XP_011520728.1:p.Ala400Thr
XM_011522427.1:c.637G>A	XP_011520729.1:p.Ala213Thr
XR_932805.1:n.2146G>A
XM_011522424.3:c.2125G>A	XP_011520726.1:p.Ala709Thr
XM_017023043.2:c.1198G>A	XP_016878532.1:p.Ala400Thr
NM_005236.3:c.1987G>A MANE Select	NP_005227.1:p.Ala663Thr