Canonical Allele Identifier: CA278485774

Gene: ERCC4

Linked Data

• dbSNP Id: rs776036851
• MyVariant Identifiers: chr16:g.14042023G>A (hg19) ; chr16:g.13948166G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948166G>A , CM000678.2:g.13948166G>A	GRCh38
NC_000016.9:g.14042023G>A , CM000678.1:g.14042023G>A	GRCh37
NC_000016.8:g.13949524G>A	NCBI36
NG_011442.1:g.33010G>A , LRG_463:g.33010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2708G>A	ENSP00000507912.1:p.Gly903Glu
ENST00000683962.1:c.*2264G>A	ENSP00000506854.1:n.*2264G>A
ENST00000311895.8:c.2570G>A MANE Select	ENSP00000310520.7:p.Gly857Glu
ENST00000311895.7:c.2570G>A	ENSP00000310520.7:p.Gly857Glu
ENST00000389138.7:n.1847G>A
NM_005236.2:c.2570G>A , LRG_463t1:c.2570G>A	NP_005227.1:p.Gly857Glu
XM_011522424.1:c.2708G>A	XP_011520726.1:p.Gly903Glu
XM_011522425.1:c.2027G>A	XP_011520727.1:p.Gly676Glu
XM_011522426.1:c.1781G>A	XP_011520728.1:p.Gly594Glu
XM_011522427.1:c.1220G>A	XP_011520729.1:p.Gly407Glu
XR_932805.1:n.2729G>A
XM_011522424.3:c.2708G>A	XP_011520726.1:p.Gly903Glu
XM_017023043.2:c.1781G>A	XP_016878532.1:p.Gly594Glu
NM_005236.3:c.2570G>A MANE Select	NP_005227.1:p.Gly857Glu