Canonical Allele Identifier: CA7910528

Gene: ERCC4

Linked Data

• dbSNP Id: rs760310698
• ExAC: 16:14029538 A / G
• gnomAD v2: 16-14029538-A-G
• gnomAD v4: 16-13935681-A-G
• MyVariant Identifiers: chr16:g.14029538A>G (hg19) ; chr16:g.13935681A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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