Canonical Allele Identifier: CA394812107

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029431A>C (hg19) ; chr16:g.13935574A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935574A>C , CM000678.2:g.13935574A>C	GRCh38
NC_000016.9:g.14029431A>C , CM000678.1:g.14029431A>C	GRCh37
NC_000016.8:g.13936932A>C	NCBI36
NG_011442.1:g.20418A>C , LRG_463:g.20418A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1720A>C
ENST00000682617.1:c.1780A>C	ENSP00000507912.1:p.Lys594Gln
ENST00000682826.1:c.*956A>C	ENSP00000507274.1:n.*956A>C
ENST00000682909.1:n.3682A>C
ENST00000683277.1:n.3287A>C
ENST00000683407.1:n.1650A>C
ENST00000683962.1:c.*1336A>C	ENSP00000506854.1:n.*1336A>C
ENST00000311895.8:c.1642A>C MANE Select	ENSP00000310520.7:p.Lys548Gln
ENST00000311895.7:c.1642A>C	ENSP00000310520.7:p.Lys548Gln
ENST00000389138.7:n.919A>C
NM_005236.2:c.1642A>C , LRG_463t1:c.1642A>C	NP_005227.1:p.Lys548Gln
XM_011522424.1:c.1780A>C	XP_011520726.1:p.Lys594Gln
XM_011522425.1:c.1099A>C	XP_011520727.1:p.Lys367Gln
XM_011522426.1:c.853A>C	XP_011520728.1:p.Lys285Gln
XM_011522427.1:c.292A>C	XP_011520729.1:p.Lys98Gln
XR_932805.1:n.1801A>C
XM_011522424.3:c.1780A>C	XP_011520726.1:p.Lys594Gln
XM_017023043.2:c.853A>C	XP_016878532.1:p.Lys285Gln
NM_005236.3:c.1642A>C MANE Select	NP_005227.1:p.Lys548Gln