Canonical Allele Identifier: CA493689836

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029355A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935498A>C , CM000678.2:g.13935498A>C	GRCh38
NC_000016.9:g.14029355A>C , CM000678.1:g.14029355A>C	GRCh37
NC_000016.8:g.13936856A>C	NCBI36
NG_011442.1:g.20342A>C , LRG_463:g.20342A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1644A>C
ENST00000682617.1:c.1704A>C	ENSP00000507912.1:p.Pro568=
ENST00000682826.1:c.*880A>C	ENSP00000507274.1:n.*880A>C
ENST00000682909.1:n.3606A>C
ENST00000683277.1:n.3211A>C
ENST00000683407.1:n.1574A>C
ENST00000683962.1:c.*1260A>C	ENSP00000506854.1:n.*1260A>C
ENST00000311895.8:c.1566A>C MANE Select	ENSP00000310520.7:p.Pro522=
ENST00000311895.7:c.1566A>C	ENSP00000310520.7:p.Pro522=
ENST00000389138.7:n.843A>C
NM_005236.2:c.1566A>C , LRG_463t1:c.1566A>C	NP_005227.1:p.Pro522=
XM_011522424.1:c.1704A>C	XP_011520726.1:p.Pro568=
XM_011522425.1:c.1023A>C	XP_011520727.1:p.Pro341=
XM_011522426.1:c.777A>C	XP_011520728.1:p.Pro259=
XM_011522427.1:c.216A>C	XP_011520729.1:p.Pro72=
XR_932805.1:n.1725A>C
XM_011522424.3:c.1704A>C	XP_011520726.1:p.Pro568=
XM_017023043.2:c.777A>C	XP_016878532.1:p.Pro259=
NM_005236.3:c.1566A>C MANE Select	NP_005227.1:p.Pro522=