Canonical Allele Identifier: CA394818091

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038666A>G (hg19) ; chr16:g.13944809A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944809A>G , CM000678.2:g.13944809A>G	GRCh38
NC_000016.9:g.14038666A>G , CM000678.1:g.14038666A>G	GRCh37
NC_000016.8:g.13946167A>G	NCBI36
NG_011442.1:g.29653A>G , LRG_463:g.29653A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2129A>G	ENSP00000507912.1:p.Asp710Gly
ENST00000683962.1:c.*1685A>G	ENSP00000506854.1:n.*1685A>G
ENST00000311895.8:c.1991A>G MANE Select	ENSP00000310520.7:p.Asp664Gly
ENST00000311895.7:c.1991A>G	ENSP00000310520.7:p.Asp664Gly
ENST00000389138.7:n.1268A>G
ENST00000462862.1:c.304A>G	ENSP00000461322.1:n.304A>G
NM_005236.2:c.1991A>G , LRG_463t1:c.1991A>G	NP_005227.1:p.Asp664Gly
XM_011522424.1:c.2129A>G	XP_011520726.1:p.Asp710Gly
XM_011522425.1:c.1448A>G	XP_011520727.1:p.Asp483Gly
XM_011522426.1:c.1202A>G	XP_011520728.1:p.Asp401Gly
XM_011522427.1:c.641A>G	XP_011520729.1:p.Asp214Gly
XR_932805.1:n.2150A>G
XM_011522424.3:c.2129A>G	XP_011520726.1:p.Asp710Gly
XM_017023043.2:c.1202A>G	XP_016878532.1:p.Asp401Gly
NM_005236.3:c.1991A>G MANE Select	NP_005227.1:p.Asp664Gly