Canonical Allele Identifier: CA394812835

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029587G>T (hg19) ; chr16:g.13935730G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935730G>T , CM000678.2:g.13935730G>T	GRCh38
NC_000016.9:g.14029587G>T , CM000678.1:g.14029587G>T	GRCh37
NC_000016.8:g.13937088G>T	NCBI36
NG_011442.1:g.20574G>T , LRG_463:g.20574G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1876G>T
ENST00000682617.1:c.1936G>T	ENSP00000507912.1:p.Gly646Trp
ENST00000682826.1:c.*1112G>T	ENSP00000507274.1:n.*1112G>T
ENST00000682909.1:n.3838G>T
ENST00000683277.1:n.3443G>T
ENST00000683407.1:n.1806G>T
ENST00000683962.1:c.*1492G>T	ENSP00000506854.1:n.*1492G>T
ENST00000311895.8:c.1798G>T MANE Select	ENSP00000310520.7:p.Gly600Trp
ENST00000311895.7:c.1798G>T	ENSP00000310520.7:p.Gly600Trp
ENST00000389138.7:n.1075G>T
NM_005236.2:c.1798G>T , LRG_463t1:c.1798G>T	NP_005227.1:p.Gly600Trp
XM_011522424.1:c.1936G>T	XP_011520726.1:p.Gly646Trp
XM_011522425.1:c.1255G>T	XP_011520727.1:p.Gly419Trp
XM_011522426.1:c.1009G>T	XP_011520728.1:p.Gly337Trp
XM_011522427.1:c.448G>T	XP_011520729.1:p.Gly150Trp
XR_932805.1:n.1957G>T
XM_011522424.3:c.1936G>T	XP_011520726.1:p.Gly646Trp
XM_017023043.2:c.1009G>T	XP_016878532.1:p.Gly337Trp
NM_005236.3:c.1798G>T MANE Select	NP_005227.1:p.Gly600Trp