Canonical Allele Identifier: CA493689556

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029538A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935681A>T , CM000678.2:g.13935681A>T	GRCh38
NC_000016.9:g.14029538A>T , CM000678.1:g.14029538A>T	GRCh37
NC_000016.8:g.13937039A>T	NCBI36
NG_011442.1:g.20525A>T , LRG_463:g.20525A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1827A>T
ENST00000682617.1:c.1887A>T	ENSP00000507912.1:p.Ala629=
ENST00000682826.1:c.*1063A>T	ENSP00000507274.1:n.*1063A>T
ENST00000682909.1:n.3789A>T
ENST00000683277.1:n.3394A>T
ENST00000683407.1:n.1757A>T
ENST00000683962.1:c.*1443A>T	ENSP00000506854.1:n.*1443A>T
ENST00000311895.8:c.1749A>T MANE Select	ENSP00000310520.7:p.Ala583=
ENST00000311895.7:c.1749A>T	ENSP00000310520.7:p.Ala583=
ENST00000389138.7:n.1026A>T
NM_005236.2:c.1749A>T , LRG_463t1:c.1749A>T	NP_005227.1:p.Ala583=
XM_011522424.1:c.1887A>T	XP_011520726.1:p.Ala629=
XM_011522425.1:c.1206A>T	XP_011520727.1:p.Ala402=
XM_011522426.1:c.960A>T	XP_011520728.1:p.Ala320=
XM_011522427.1:c.399A>T	XP_011520729.1:p.Ala133=
XR_932805.1:n.1908A>T
XM_011522424.3:c.1887A>T	XP_011520726.1:p.Ala629=
XM_017023043.2:c.960A>T	XP_016878532.1:p.Ala320=
NM_005236.3:c.1749A>T MANE Select	NP_005227.1:p.Ala583=