Canonical Allele Identifier: CA493689515

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141607966
• MyVariant Identifiers: chr16:g.14029475C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935618C>T , CM000678.2:g.13935618C>T	GRCh38
NC_000016.9:g.14029475C>T , CM000678.1:g.14029475C>T	GRCh37
NC_000016.8:g.13936976C>T	NCBI36
NG_011442.1:g.20462C>T , LRG_463:g.20462C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1764C>T
ENST00000682617.1:c.1824C>T	ENSP00000507912.1:p.Asp608=
ENST00000682826.1:c.*1000C>T	ENSP00000507274.1:n.*1000C>T
ENST00000682909.1:n.3726C>T
ENST00000683277.1:n.3331C>T
ENST00000683407.1:n.1694C>T
ENST00000683962.1:c.*1380C>T	ENSP00000506854.1:n.*1380C>T
ENST00000311895.8:c.1686C>T MANE Select	ENSP00000310520.7:p.Asp562=
ENST00000311895.7:c.1686C>T	ENSP00000310520.7:p.Asp562=
ENST00000389138.7:n.963C>T
NM_005236.2:c.1686C>T , LRG_463t1:c.1686C>T	NP_005227.1:p.Asp562=
XM_011522424.1:c.1824C>T	XP_011520726.1:p.Asp608=
XM_011522425.1:c.1143C>T	XP_011520727.1:p.Asp381=
XM_011522426.1:c.897C>T	XP_011520728.1:p.Asp299=
XM_011522427.1:c.336C>T	XP_011520729.1:p.Asp112=
XR_932805.1:n.1845C>T
XM_011522424.3:c.1824C>T	XP_011520726.1:p.Asp608=
XM_017023043.2:c.897C>T	XP_016878532.1:p.Asp299=
NM_005236.3:c.1686C>T MANE Select	NP_005227.1:p.Asp562=