Canonical Allele Identifier: CA394823335

Gene: ERCC4

Linked Data

• COSMIC: COSM1251465
• MyVariant Identifiers: chr16:g.14041836T>G (hg19) ; chr16:g.13947979T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947979T>G , CM000678.2:g.13947979T>G	GRCh38
NC_000016.9:g.14041836T>G , CM000678.1:g.14041836T>G	GRCh37
NC_000016.8:g.13949337T>G	NCBI36
NG_011442.1:g.32823T>G , LRG_463:g.32823T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2521T>G	ENSP00000507912.1:p.Phe841Val
ENST00000683962.1:c.*2077T>G	ENSP00000506854.1:n.*2077T>G
ENST00000311895.8:c.2383T>G MANE Select	ENSP00000310520.7:p.Phe795Val
ENST00000311895.7:c.2383T>G	ENSP00000310520.7:p.Phe795Val
ENST00000389138.7:n.1660T>G
ENST00000462862.1:c.696T>G	ENSP00000461322.1:n.696T>G
NM_005236.2:c.2383T>G , LRG_463t1:c.2383T>G	NP_005227.1:p.Phe795Val
XM_011522424.1:c.2521T>G	XP_011520726.1:p.Phe841Val
XM_011522425.1:c.1840T>G	XP_011520727.1:p.Phe614Val
XM_011522426.1:c.1594T>G	XP_011520728.1:p.Phe532Val
XM_011522427.1:c.1033T>G	XP_011520729.1:p.Phe345Val
XR_932805.1:n.2542T>G
XM_011522424.3:c.2521T>G	XP_011520726.1:p.Phe841Val
XM_017023043.2:c.1594T>G	XP_016878532.1:p.Phe532Val
NM_005236.3:c.2383T>G MANE Select	NP_005227.1:p.Phe795Val