Canonical Allele Identifier: CA493689880

Gene: ERCC4

Linked Data

• dbSNP Id: rs1217460973
• MyVariant Identifiers: chr16:g.14029439C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935582C>A , CM000678.2:g.13935582C>A	GRCh38
NC_000016.9:g.14029439C>A , CM000678.1:g.14029439C>A	GRCh37
NC_000016.8:g.13936940C>A	NCBI36
NG_011442.1:g.20426C>A , LRG_463:g.20426C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1728C>A
ENST00000682617.1:c.1788C>A	ENSP00000507912.1:p.Pro596=
ENST00000682826.1:c.*964C>A	ENSP00000507274.1:n.*964C>A
ENST00000682909.1:n.3690C>A
ENST00000683277.1:n.3295C>A
ENST00000683407.1:n.1658C>A
ENST00000683962.1:c.*1344C>A	ENSP00000506854.1:n.*1344C>A
ENST00000311895.8:c.1650C>A MANE Select	ENSP00000310520.7:p.Pro550=
ENST00000311895.7:c.1650C>A	ENSP00000310520.7:p.Pro550=
ENST00000389138.7:n.927C>A
NM_005236.2:c.1650C>A , LRG_463t1:c.1650C>A	NP_005227.1:p.Pro550=
XM_011522424.1:c.1788C>A	XP_011520726.1:p.Pro596=
XM_011522425.1:c.1107C>A	XP_011520727.1:p.Pro369=
XM_011522426.1:c.861C>A	XP_011520728.1:p.Pro287=
XM_011522427.1:c.300C>A	XP_011520729.1:p.Pro100=
XR_932805.1:n.1809C>A
XM_011522424.3:c.1788C>A	XP_011520726.1:p.Pro596=
XM_017023043.2:c.861C>A	XP_016878532.1:p.Pro287=
NM_005236.3:c.1650C>A MANE Select	NP_005227.1:p.Pro550=