Canonical Allele Identifier: CA394812114

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029432A>C (hg19) ; chr16:g.13935575A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935575A>C , CM000678.2:g.13935575A>C	GRCh38
NC_000016.9:g.14029432A>C , CM000678.1:g.14029432A>C	GRCh37
NC_000016.8:g.13936933A>C	NCBI36
NG_011442.1:g.20419A>C , LRG_463:g.20419A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682568.1:n.1721A>C
ENST00000682617.1:c.1781A>C	ENSP00000507912.1:p.Lys594Thr
ENST00000682826.1:c.*957A>C	ENSP00000507274.1:n.*957A>C
ENST00000682909.1:n.3683A>C
ENST00000683277.1:n.3288A>C
ENST00000683407.1:n.1651A>C
ENST00000683962.1:c.*1337A>C	ENSP00000506854.1:n.*1337A>C
ENST00000311895.8:c.1643A>C MANE Select	ENSP00000310520.7:p.Lys548Thr
ENST00000311895.7:c.1643A>C	ENSP00000310520.7:p.Lys548Thr
ENST00000389138.7:n.920A>C
NM_005236.2:c.1643A>C , LRG_463t1:c.1643A>C	NP_005227.1:p.Lys548Thr
XM_011522424.1:c.1781A>C	XP_011520726.1:p.Lys594Thr
XM_011522425.1:c.1100A>C	XP_011520727.1:p.Lys367Thr
XM_011522426.1:c.854A>C	XP_011520728.1:p.Lys285Thr
XM_011522427.1:c.293A>C	XP_011520729.1:p.Lys98Thr
XR_932805.1:n.1802A>C
XM_011522424.3:c.1781A>C	XP_011520726.1:p.Lys594Thr
XM_017023043.2:c.854A>C	XP_016878532.1:p.Lys285Thr
NM_005236.3:c.1643A>C MANE Select	NP_005227.1:p.Lys548Thr