Canonical Allele Identifier: CA394822531

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141620164
• MyVariant Identifiers: chr16:g.14041666A>C (hg19) ; chr16:g.13947809A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947809A>C , CM000678.2:g.13947809A>C	GRCh38
NC_000016.9:g.14041666A>C , CM000678.1:g.14041666A>C	GRCh37
NC_000016.8:g.13949167A>C	NCBI36
NG_011442.1:g.32653A>C , LRG_463:g.32653A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2351A>C	ENSP00000507912.1:p.Asn784Thr
ENST00000683962.1:c.*1907A>C	ENSP00000506854.1:n.*1907A>C
ENST00000311895.8:c.2213A>C MANE Select	ENSP00000310520.7:p.Asn738Thr
ENST00000311895.7:c.2213A>C	ENSP00000310520.7:p.Asn738Thr
ENST00000389138.7:n.1490A>C
ENST00000462862.1:c.526A>C	ENSP00000461322.1:n.526A>C
NM_005236.2:c.2213A>C , LRG_463t1:c.2213A>C	NP_005227.1:p.Asn738Thr
XM_011522424.1:c.2351A>C	XP_011520726.1:p.Asn784Thr
XM_011522425.1:c.1670A>C	XP_011520727.1:p.Asn557Thr
XM_011522426.1:c.1424A>C	XP_011520728.1:p.Asn475Thr
XM_011522427.1:c.863A>C	XP_011520729.1:p.Asn288Thr
XR_932805.1:n.2372A>C
XM_011522424.3:c.2351A>C	XP_011520726.1:p.Asn784Thr
XM_017023043.2:c.1424A>C	XP_016878532.1:p.Asn475Thr
NM_005236.3:c.2213A>C MANE Select	NP_005227.1:p.Asn738Thr