Canonical Allele Identifier: CA394812929

Gene: ERCC4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935745C>A , CM000678.2:g.13935745C>A	GRCh38
NC_000016.9:g.14029602C>A , CM000678.1:g.14029602C>A	GRCh37
NC_000016.8:g.13937103C>A	NCBI36
NG_011442.1:g.20589C>A , LRG_463:g.20589C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1891C>A
ENST00000682617.1:c.1949+2C>A	ENSP00000507912.1:n.1949+2C>A
ENST00000682826.1:c.*1125+2C>A	ENSP00000507274.1:n.*1125+2C>A
ENST00000682909.1:n.3851+2C>A
ENST00000683277.1:n.3456+2C>A
ENST00000683407.1:n.1821C>A
ENST00000683962.1:c.*1505+2C>A	ENSP00000506854.1:n.*1505+2C>A
ENST00000311895.8:c.1811+2C>A MANE Select	ENSP00000310520.7:n.1811+2C>A
ENST00000311895.7:c.1811+2C>A	ENSP00000310520.7:n.1811+2C>A
ENST00000389138.7:n.1088+2C>A
NM_005236.2:c.1811+2C>A , LRG_463t1:c.1811+2C>A	NP_005227.1:n.1811+2C>A
XM_011522424.1:c.1949+2C>A	XP_011520726.1:n.1949+2C>A
XM_011522425.1:c.1268+2C>A	XP_011520727.1:n.1268+2C>A
XM_011522426.1:c.1022+2C>A	XP_011520728.1:n.1022+2C>A
XM_011522427.1:c.461+2C>A	XP_011520729.1:n.461+2C>A
XR_932805.1:n.1970+2C>A
XM_011522424.3:c.1949+2C>A	XP_011520726.1:n.1949+2C>A
XM_017023043.2:c.1022+2C>A	XP_016878532.1:n.1022+2C>A
NM_005236.3:c.1811+2C>A MANE Select	NP_005227.1:n.1811+2C>A