Canonical Allele Identifier: CA394822426

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041646T>G (hg19) ; chr16:g.13947789T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947789T>G , CM000678.2:g.13947789T>G	GRCh38
NC_000016.9:g.14041646T>G , CM000678.1:g.14041646T>G	GRCh37
NC_000016.8:g.13949147T>G	NCBI36
NG_011442.1:g.32633T>G , LRG_463:g.32633T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2331T>G	ENSP00000507912.1:p.Asp777Glu
ENST00000683962.1:c.*1887T>G	ENSP00000506854.1:n.*1887T>G
ENST00000311895.8:c.2193T>G MANE Select	ENSP00000310520.7:p.Asp731Glu
ENST00000311895.7:c.2193T>G	ENSP00000310520.7:p.Asp731Glu
ENST00000389138.7:n.1470T>G
ENST00000462862.1:c.506T>G	ENSP00000461322.1:n.506T>G
NM_005236.2:c.2193T>G , LRG_463t1:c.2193T>G	NP_005227.1:p.Asp731Glu
XM_011522424.1:c.2331T>G	XP_011520726.1:p.Asp777Glu
XM_011522425.1:c.1650T>G	XP_011520727.1:p.Asp550Glu
XM_011522426.1:c.1404T>G	XP_011520728.1:p.Asp468Glu
XM_011522427.1:c.843T>G	XP_011520729.1:p.Asp281Glu
XR_932805.1:n.2352T>G
XM_011522424.3:c.2331T>G	XP_011520726.1:p.Asp777Glu
XM_017023043.2:c.1404T>G	XP_016878532.1:p.Asp468Glu
NM_005236.3:c.2193T>G MANE Select	NP_005227.1:p.Asp731Glu