Canonical Allele Identifier: CA394812432

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029479T>G (hg19) ; chr16:g.13935622T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935622T>G , CM000678.2:g.13935622T>G	GRCh38
NC_000016.9:g.14029479T>G , CM000678.1:g.14029479T>G	GRCh37
NC_000016.8:g.13936980T>G	NCBI36
NG_011442.1:g.20466T>G , LRG_463:g.20466T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1768T>G
ENST00000682617.1:c.1828T>G	ENSP00000507912.1:p.Tyr610Asp
ENST00000682826.1:c.*1004T>G	ENSP00000507274.1:n.*1004T>G
ENST00000682909.1:n.3730T>G
ENST00000683277.1:n.3335T>G
ENST00000683407.1:n.1698T>G
ENST00000683962.1:c.*1384T>G	ENSP00000506854.1:n.*1384T>G
ENST00000311895.8:c.1690T>G MANE Select	ENSP00000310520.7:p.Tyr564Asp
ENST00000311895.7:c.1690T>G	ENSP00000310520.7:p.Tyr564Asp
ENST00000389138.7:n.967T>G
NM_005236.2:c.1690T>G , LRG_463t1:c.1690T>G	NP_005227.1:p.Tyr564Asp
XM_011522424.1:c.1828T>G	XP_011520726.1:p.Tyr610Asp
XM_011522425.1:c.1147T>G	XP_011520727.1:p.Tyr383Asp
XM_011522426.1:c.901T>G	XP_011520728.1:p.Tyr301Asp
XM_011522427.1:c.340T>G	XP_011520729.1:p.Tyr114Asp
XR_932805.1:n.1849T>G
XM_011522424.3:c.1828T>G	XP_011520726.1:p.Tyr610Asp
XM_017023043.2:c.901T>G	XP_016878532.1:p.Tyr301Asp
NM_005236.3:c.1690T>G MANE Select	NP_005227.1:p.Tyr564Asp