Canonical Allele Identifier: CA394817674

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038625T>G (hg19) ; chr16:g.13944768T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944768T>G , CM000678.2:g.13944768T>G	GRCh38
NC_000016.9:g.14038625T>G , CM000678.1:g.14038625T>G	GRCh37
NC_000016.8:g.13946126T>G	NCBI36
NG_011442.1:g.29612T>G , LRG_463:g.29612T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2088T>G	ENSP00000507912.1:p.Asp696Glu
ENST00000683962.1:c.*1644T>G	ENSP00000506854.1:n.*1644T>G
ENST00000311895.8:c.1950T>G MANE Select	ENSP00000310520.7:p.Asp650Glu
ENST00000311895.7:c.1950T>G	ENSP00000310520.7:p.Asp650Glu
ENST00000389138.7:n.1227T>G
ENST00000462862.1:c.263T>G	ENSP00000461322.1:n.263T>G
NM_005236.2:c.1950T>G , LRG_463t1:c.1950T>G	NP_005227.1:p.Asp650Glu
XM_011522424.1:c.2088T>G	XP_011520726.1:p.Asp696Glu
XM_011522425.1:c.1407T>G	XP_011520727.1:p.Asp469Glu
XM_011522426.1:c.1161T>G	XP_011520728.1:p.Asp387Glu
XM_011522427.1:c.600T>G	XP_011520729.1:p.Asp200Glu
XR_932805.1:n.2109T>G
XM_011522424.3:c.2088T>G	XP_011520726.1:p.Asp696Glu
XM_017023043.2:c.1161T>G	XP_016878532.1:p.Asp387Glu
NM_005236.3:c.1950T>G MANE Select	NP_005227.1:p.Asp650Glu