Canonical Allele Identifier: CA394824518

Gene: ERCC4

Linked Data

• dbSNP Id: rs749822053
• MyVariant Identifiers: chr16:g.14042041G>A (hg19) ; chr16:g.13948184G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948184G>A , CM000678.2:g.13948184G>A	GRCh38
NC_000016.9:g.14042041G>A , CM000678.1:g.14042041G>A	GRCh37
NC_000016.8:g.13949542G>A	NCBI36
NG_011442.1:g.33028G>A , LRG_463:g.33028G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2726G>A	ENSP00000507912.1:p.Cys909Tyr
ENST00000683962.1:c.*2282G>A	ENSP00000506854.1:n.*2282G>A
ENST00000311895.8:c.2588G>A MANE Select	ENSP00000310520.7:p.Cys863Tyr
ENST00000311895.7:c.2588G>A	ENSP00000310520.7:p.Cys863Tyr
ENST00000389138.7:n.1865G>A
NM_005236.2:c.2588G>A , LRG_463t1:c.2588G>A	NP_005227.1:p.Cys863Tyr
XM_011522424.1:c.2726G>A	XP_011520726.1:p.Cys909Tyr
XM_011522425.1:c.2045G>A	XP_011520727.1:p.Cys682Tyr
XM_011522426.1:c.1799G>A	XP_011520728.1:p.Cys600Tyr
XM_011522427.1:c.1238G>A	XP_011520729.1:p.Cys413Tyr
XR_932805.1:n.2747G>A
XM_011522424.3:c.2726G>A	XP_011520726.1:p.Cys909Tyr
XM_017023043.2:c.1799G>A	XP_016878532.1:p.Cys600Tyr
NM_005236.3:c.2588G>A MANE Select	NP_005227.1:p.Cys863Tyr