Canonical Allele Identifier: CA394812470

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13935634-A-G
• MyVariant Identifiers: chr16:g.14029491A>G (hg19) ; chr16:g.13935634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935634A>G , CM000678.2:g.13935634A>G	GRCh38
NC_000016.9:g.14029491A>G , CM000678.1:g.14029491A>G	GRCh37
NC_000016.8:g.13936992A>G	NCBI36
NG_011442.1:g.20478A>G , LRG_463:g.20478A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1780A>G
ENST00000682617.1:c.1840A>G	ENSP00000507912.1:p.Arg614Gly
ENST00000682826.1:c.*1016A>G	ENSP00000507274.1:n.*1016A>G
ENST00000682909.1:n.3742A>G
ENST00000683277.1:n.3347A>G
ENST00000683407.1:n.1710A>G
ENST00000683962.1:c.*1396A>G	ENSP00000506854.1:n.*1396A>G
ENST00000311895.8:c.1702A>G MANE Select	ENSP00000310520.7:p.Arg568Gly
ENST00000311895.7:c.1702A>G	ENSP00000310520.7:p.Arg568Gly
ENST00000389138.7:n.979A>G
NM_005236.2:c.1702A>G , LRG_463t1:c.1702A>G	NP_005227.1:p.Arg568Gly
XM_011522424.1:c.1840A>G	XP_011520726.1:p.Arg614Gly
XM_011522425.1:c.1159A>G	XP_011520727.1:p.Arg387Gly
XM_011522426.1:c.913A>G	XP_011520728.1:p.Arg305Gly
XM_011522427.1:c.352A>G	XP_011520729.1:p.Arg118Gly
XR_932805.1:n.1861A>G
XM_011522424.3:c.1840A>G	XP_011520726.1:p.Arg614Gly
XM_017023043.2:c.913A>G	XP_016878532.1:p.Arg305Gly
NM_005236.3:c.1702A>G MANE Select	NP_005227.1:p.Arg568Gly