Canonical Allele Identifier: CA394823152

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041807G>C (hg19) ; chr16:g.13947950G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947950G>C , CM000678.2:g.13947950G>C	GRCh38
NC_000016.9:g.14041807G>C , CM000678.1:g.14041807G>C	GRCh37
NC_000016.8:g.13949308G>C	NCBI36
NG_011442.1:g.32794G>C , LRG_463:g.32794G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2492G>C	ENSP00000507912.1:p.Ser831Thr
ENST00000683962.1:c.*2048G>C	ENSP00000506854.1:n.*2048G>C
ENST00000311895.8:c.2354G>C MANE Select	ENSP00000310520.7:p.Ser785Thr
ENST00000311895.7:c.2354G>C	ENSP00000310520.7:p.Ser785Thr
ENST00000389138.7:n.1631G>C
ENST00000462862.1:c.667G>C	ENSP00000461322.1:n.667G>C
NM_005236.2:c.2354G>C , LRG_463t1:c.2354G>C	NP_005227.1:p.Ser785Thr
XM_011522424.1:c.2492G>C	XP_011520726.1:p.Ser831Thr
XM_011522425.1:c.1811G>C	XP_011520727.1:p.Ser604Thr
XM_011522426.1:c.1565G>C	XP_011520728.1:p.Ser522Thr
XM_011522427.1:c.1004G>C	XP_011520729.1:p.Ser335Thr
XR_932805.1:n.2513G>C
XM_011522424.3:c.2492G>C	XP_011520726.1:p.Ser831Thr
XM_017023043.2:c.1565G>C	XP_016878532.1:p.Ser522Thr
NM_005236.3:c.2354G>C MANE Select	NP_005227.1:p.Ser785Thr