Canonical Allele Identifier: CA394811452

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029323G>T (hg19) ; chr16:g.13935466G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935466G>T , CM000678.2:g.13935466G>T	GRCh38
NC_000016.9:g.14029323G>T , CM000678.1:g.14029323G>T	GRCh37
NC_000016.8:g.13936824G>T	NCBI36
NG_011442.1:g.20310G>T , LRG_463:g.20310G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1612G>T
ENST00000682617.1:c.1672G>T	ENSP00000507912.1:p.Glu558Ter
ENST00000682826.1:c.*848G>T	ENSP00000507274.1:n.*848G>T
ENST00000682909.1:n.3574G>T
ENST00000683277.1:n.3179G>T
ENST00000683407.1:n.1542G>T
ENST00000683962.1:c.*1228G>T	ENSP00000506854.1:n.*1228G>T
ENST00000311895.8:c.1534G>T MANE Select	ENSP00000310520.7:p.Glu512Ter
ENST00000311895.7:c.1534G>T	ENSP00000310520.7:p.Glu512Ter
ENST00000389138.7:n.811G>T
NM_005236.2:c.1534G>T , LRG_463t1:c.1534G>T	NP_005227.1:p.Glu512Ter
XM_011522424.1:c.1672G>T	XP_011520726.1:p.Glu558Ter
XM_011522425.1:c.991G>T	XP_011520727.1:p.Glu331Ter
XM_011522426.1:c.745G>T	XP_011520728.1:p.Glu249Ter
XM_011522427.1:c.184G>T	XP_011520729.1:p.Glu62Ter
XR_932805.1:n.1693G>T
XM_011522424.3:c.1672G>T	XP_011520726.1:p.Glu558Ter
XM_017023043.2:c.745G>T	XP_016878532.1:p.Glu249Ter
NM_005236.3:c.1534G>T MANE Select	NP_005227.1:p.Glu512Ter