Canonical Allele Identifier: CA7910756

Gene: ERCC4

Linked Data

• dbSNP Id: rs749688539
• ExAC: 16:14041959 G / A
• gnomAD v2: 16-14041959-G-A
• gnomAD v3: 16-13948102-G-A
• gnomAD v4: 16-13948102-G-A
• COSMIC: COSM6078370
• MyVariant Identifiers: chr16:g.14041959G>A (hg19) ; chr16:g.13948102G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948102G>A , CM000678.2:g.13948102G>A	GRCh38
NC_000016.9:g.14041959G>A , CM000678.1:g.14041959G>A	GRCh37
NC_000016.8:g.13949460G>A	NCBI36
NG_011442.1:g.32946G>A , LRG_463:g.32946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2644G>A	ENSP00000507912.1:p.Glu882Lys
ENST00000683962.1:c.*2200G>A	ENSP00000506854.1:n.*2200G>A
ENST00000311895.8:c.2506G>A MANE Select	ENSP00000310520.7:p.Glu836Lys
ENST00000311895.7:c.2506G>A	ENSP00000310520.7:p.Glu836Lys
ENST00000389138.7:n.1783G>A
NM_005236.2:c.2506G>A , LRG_463t1:c.2506G>A	NP_005227.1:p.Glu836Lys
XM_011522424.1:c.2644G>A	XP_011520726.1:p.Glu882Lys
XM_011522425.1:c.1963G>A	XP_011520727.1:p.Glu655Lys
XM_011522426.1:c.1717G>A	XP_011520728.1:p.Glu573Lys
XM_011522427.1:c.1156G>A	XP_011520729.1:p.Glu386Lys
XR_932805.1:n.2665G>A
XM_011522424.3:c.2644G>A	XP_011520726.1:p.Glu882Lys
XM_017023043.2:c.1717G>A	XP_016878532.1:p.Glu573Lys
NM_005236.3:c.2506G>A MANE Select	NP_005227.1:p.Glu836Lys