Canonical Allele Identifier: CA493690025

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041829A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947972A>G , CM000678.2:g.13947972A>G	GRCh38
NC_000016.9:g.14041829A>G , CM000678.1:g.14041829A>G	GRCh37
NC_000016.8:g.13949330A>G	NCBI36
NG_011442.1:g.32816A>G , LRG_463:g.32816A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2514A>G	ENSP00000507912.1:p.Thr838=
ENST00000683962.1:c.*2070A>G	ENSP00000506854.1:n.*2070A>G
ENST00000311895.8:c.2376A>G MANE Select	ENSP00000310520.7:p.Thr792=
ENST00000311895.7:c.2376A>G	ENSP00000310520.7:p.Thr792=
ENST00000389138.7:n.1653A>G
ENST00000462862.1:c.689A>G	ENSP00000461322.1:n.689A>G
NM_005236.2:c.2376A>G , LRG_463t1:c.2376A>G	NP_005227.1:p.Thr792=
XM_011522424.1:c.2514A>G	XP_011520726.1:p.Thr838=
XM_011522425.1:c.1833A>G	XP_011520727.1:p.Thr611=
XM_011522426.1:c.1587A>G	XP_011520728.1:p.Thr529=
XM_011522427.1:c.1026A>G	XP_011520729.1:p.Thr342=
XR_932805.1:n.2535A>G
XM_011522424.3:c.2514A>G	XP_011520726.1:p.Thr838=
XM_017023043.2:c.1587A>G	XP_016878532.1:p.Thr529=
NM_005236.3:c.2376A>G MANE Select	NP_005227.1:p.Thr792=