Canonical Allele Identifier: CA394824270

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041973G>C (hg19) ; chr16:g.13948116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948116G>C , CM000678.2:g.13948116G>C	GRCh38
NC_000016.9:g.14041973G>C , CM000678.1:g.14041973G>C	GRCh37
NC_000016.8:g.13949474G>C	NCBI36
NG_011442.1:g.32960G>C , LRG_463:g.32960G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2658G>C	ENSP00000507912.1:p.Glu886Asp
ENST00000683962.1:c.*2214G>C	ENSP00000506854.1:n.*2214G>C
ENST00000311895.8:c.2520G>C MANE Select	ENSP00000310520.7:p.Glu840Asp
ENST00000311895.7:c.2520G>C	ENSP00000310520.7:p.Glu840Asp
ENST00000389138.7:n.1797G>C
NM_005236.2:c.2520G>C , LRG_463t1:c.2520G>C	NP_005227.1:p.Glu840Asp
XM_011522424.1:c.2658G>C	XP_011520726.1:p.Glu886Asp
XM_011522425.1:c.1977G>C	XP_011520727.1:p.Glu659Asp
XM_011522426.1:c.1731G>C	XP_011520728.1:p.Glu577Asp
XM_011522427.1:c.1170G>C	XP_011520729.1:p.Glu390Asp
XR_932805.1:n.2679G>C
XM_011522424.3:c.2658G>C	XP_011520726.1:p.Glu886Asp
XM_017023043.2:c.1731G>C	XP_016878532.1:p.Glu577Asp
NM_005236.3:c.2520G>C MANE Select	NP_005227.1:p.Glu840Asp