Canonical Allele Identifier: CA394812455

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029483C>A (hg19) ; chr16:g.13935626C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935626C>A , CM000678.2:g.13935626C>A	GRCh38
NC_000016.9:g.14029483C>A , CM000678.1:g.14029483C>A	GRCh37
NC_000016.8:g.13936984C>A	NCBI36
NG_011442.1:g.20470C>A , LRG_463:g.20470C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1772C>A
ENST00000682617.1:c.1832C>A	ENSP00000507912.1:p.Ala611Asp
ENST00000682826.1:c.*1008C>A	ENSP00000507274.1:n.*1008C>A
ENST00000682909.1:n.3734C>A
ENST00000683277.1:n.3339C>A
ENST00000683407.1:n.1702C>A
ENST00000683962.1:c.*1388C>A	ENSP00000506854.1:n.*1388C>A
ENST00000311895.8:c.1694C>A MANE Select	ENSP00000310520.7:p.Ala565Asp
ENST00000311895.7:c.1694C>A	ENSP00000310520.7:p.Ala565Asp
ENST00000389138.7:n.971C>A
NM_005236.2:c.1694C>A , LRG_463t1:c.1694C>A	NP_005227.1:p.Ala565Asp
XM_011522424.1:c.1832C>A	XP_011520726.1:p.Ala611Asp
XM_011522425.1:c.1151C>A	XP_011520727.1:p.Ala384Asp
XM_011522426.1:c.905C>A	XP_011520728.1:p.Ala302Asp
XM_011522427.1:c.344C>A	XP_011520729.1:p.Ala115Asp
XR_932805.1:n.1853C>A
XM_011522424.3:c.1832C>A	XP_011520726.1:p.Ala611Asp
XM_017023043.2:c.905C>A	XP_016878532.1:p.Ala302Asp
NM_005236.3:c.1694C>A MANE Select	NP_005227.1:p.Ala565Asp