Canonical Allele Identifier: CA394824794

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14042110G>C (hg19) ; chr16:g.13948253G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948253G>C , CM000678.2:g.13948253G>C	GRCh38
NC_000016.9:g.14042110G>C , CM000678.1:g.14042110G>C	GRCh37
NC_000016.8:g.13949611G>C	NCBI36
NG_011442.1:g.33097G>C , LRG_463:g.33097G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2795G>C	ENSP00000507912.1:p.Ser932Thr
ENST00000683962.1:c.*2351G>C	ENSP00000506854.1:n.*2351G>C
ENST00000311895.8:c.2657G>C MANE Select	ENSP00000310520.7:p.Ser886Thr
ENST00000311895.7:c.2657G>C	ENSP00000310520.7:p.Ser886Thr
ENST00000389138.7:n.1934G>C
NM_005236.2:c.2657G>C , LRG_463t1:c.2657G>C	NP_005227.1:p.Ser886Thr
XM_011522424.1:c.2795G>C	XP_011520726.1:p.Ser932Thr
XM_011522425.1:c.2114G>C	XP_011520727.1:p.Ser705Thr
XM_011522426.1:c.1868G>C	XP_011520728.1:p.Ser623Thr
XM_011522427.1:c.1307G>C	XP_011520729.1:p.Ser436Thr
XR_932805.1:n.2816G>C
XM_011522424.3:c.2795G>C	XP_011520726.1:p.Ser932Thr
XM_017023043.2:c.1868G>C	XP_016878532.1:p.Ser623Thr
NM_005236.3:c.2657G>C MANE Select	NP_005227.1:p.Ser886Thr