Canonical Allele Identifier: CA493689871

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029424A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935567A>G , CM000678.2:g.13935567A>G	GRCh38
NC_000016.9:g.14029424A>G , CM000678.1:g.14029424A>G	GRCh37
NC_000016.8:g.13936925A>G	NCBI36
NG_011442.1:g.20411A>G , LRG_463:g.20411A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1713A>G
ENST00000682617.1:c.1773A>G	ENSP00000507912.1:p.Gly591=
ENST00000682826.1:c.*949A>G	ENSP00000507274.1:n.*949A>G
ENST00000682909.1:n.3675A>G
ENST00000683277.1:n.3280A>G
ENST00000683407.1:n.1643A>G
ENST00000683962.1:c.*1329A>G	ENSP00000506854.1:n.*1329A>G
ENST00000311895.8:c.1635A>G MANE Select	ENSP00000310520.7:p.Gly545=
ENST00000311895.7:c.1635A>G	ENSP00000310520.7:p.Gly545=
ENST00000389138.7:n.912A>G
NM_005236.2:c.1635A>G , LRG_463t1:c.1635A>G	NP_005227.1:p.Gly545=
XM_011522424.1:c.1773A>G	XP_011520726.1:p.Gly591=
XM_011522425.1:c.1092A>G	XP_011520727.1:p.Gly364=
XM_011522426.1:c.846A>G	XP_011520728.1:p.Gly282=
XM_011522427.1:c.285A>G	XP_011520729.1:p.Gly95=
XR_932805.1:n.1794A>G
XM_011522424.3:c.1773A>G	XP_011520726.1:p.Gly591=
XM_017023043.2:c.846A>G	XP_016878532.1:p.Gly282=
NM_005236.3:c.1635A>G MANE Select	NP_005227.1:p.Gly545=