Canonical Allele Identifier: CA394823123

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041795G>C (hg19) ; chr16:g.13947938G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947938G>C , CM000678.2:g.13947938G>C	GRCh38
NC_000016.9:g.14041795G>C , CM000678.1:g.14041795G>C	GRCh37
NC_000016.8:g.13949296G>C	NCBI36
NG_011442.1:g.32782G>C , LRG_463:g.32782G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2480G>C	ENSP00000507912.1:p.Ser827Thr
ENST00000683962.1:c.*2036G>C	ENSP00000506854.1:n.*2036G>C
ENST00000311895.8:c.2342G>C MANE Select	ENSP00000310520.7:p.Ser781Thr
ENST00000311895.7:c.2342G>C	ENSP00000310520.7:p.Ser781Thr
ENST00000389138.7:n.1619G>C
ENST00000462862.1:c.655G>C	ENSP00000461322.1:n.655G>C
NM_005236.2:c.2342G>C , LRG_463t1:c.2342G>C	NP_005227.1:p.Ser781Thr
XM_011522424.1:c.2480G>C	XP_011520726.1:p.Ser827Thr
XM_011522425.1:c.1799G>C	XP_011520727.1:p.Ser600Thr
XM_011522426.1:c.1553G>C	XP_011520728.1:p.Ser518Thr
XM_011522427.1:c.992G>C	XP_011520729.1:p.Ser331Thr
XR_932805.1:n.2501G>C
XM_011522424.3:c.2480G>C	XP_011520726.1:p.Ser827Thr
XM_017023043.2:c.1553G>C	XP_016878532.1:p.Ser518Thr
NM_005236.3:c.2342G>C MANE Select	NP_005227.1:p.Ser781Thr