Canonical Allele Identifier: CA394812069

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029426T>A (hg19) ; chr16:g.13935569T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935569T>A , CM000678.2:g.13935569T>A	GRCh38
NC_000016.9:g.14029426T>A , CM000678.1:g.14029426T>A	GRCh37
NC_000016.8:g.13936927T>A	NCBI36
NG_011442.1:g.20413T>A , LRG_463:g.20413T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682568.1:n.1715T>A
ENST00000682617.1:c.1775T>A	ENSP00000507912.1:p.Ile592Asn
ENST00000682826.1:c.*951T>A	ENSP00000507274.1:n.*951T>A
ENST00000682909.1:n.3677T>A
ENST00000683277.1:n.3282T>A
ENST00000683407.1:n.1645T>A
ENST00000683962.1:c.*1331T>A	ENSP00000506854.1:n.*1331T>A
ENST00000311895.8:c.1637T>A MANE Select	ENSP00000310520.7:p.Ile546Asn
ENST00000311895.7:c.1637T>A	ENSP00000310520.7:p.Ile546Asn
ENST00000389138.7:n.914T>A
NM_005236.2:c.1637T>A , LRG_463t1:c.1637T>A	NP_005227.1:p.Ile546Asn
XM_011522424.1:c.1775T>A	XP_011520726.1:p.Ile592Asn
XM_011522425.1:c.1094T>A	XP_011520727.1:p.Ile365Asn
XM_011522426.1:c.848T>A	XP_011520728.1:p.Ile283Asn
XM_011522427.1:c.287T>A	XP_011520729.1:p.Ile96Asn
XR_932805.1:n.1796T>A
XM_011522424.3:c.1775T>A	XP_011520726.1:p.Ile592Asn
XM_017023043.2:c.848T>A	XP_016878532.1:p.Ile283Asn
NM_005236.3:c.1637T>A MANE Select	NP_005227.1:p.Ile546Asn