Canonical Allele Identifier: CA394818094

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038666A>C (hg19) ; chr16:g.13944809A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944809A>C , CM000678.2:g.13944809A>C	GRCh38
NC_000016.9:g.14038666A>C , CM000678.1:g.14038666A>C	GRCh37
NC_000016.8:g.13946167A>C	NCBI36
NG_011442.1:g.29653A>C , LRG_463:g.29653A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2129A>C	ENSP00000507912.1:p.Asp710Ala
ENST00000683962.1:c.*1685A>C	ENSP00000506854.1:n.*1685A>C
ENST00000311895.8:c.1991A>C MANE Select	ENSP00000310520.7:p.Asp664Ala
ENST00000311895.7:c.1991A>C	ENSP00000310520.7:p.Asp664Ala
ENST00000389138.7:n.1268A>C
ENST00000462862.1:c.304A>C	ENSP00000461322.1:n.304A>C
NM_005236.2:c.1991A>C , LRG_463t1:c.1991A>C	NP_005227.1:p.Asp664Ala
XM_011522424.1:c.2129A>C	XP_011520726.1:p.Asp710Ala
XM_011522425.1:c.1448A>C	XP_011520727.1:p.Asp483Ala
XM_011522426.1:c.1202A>C	XP_011520728.1:p.Asp401Ala
XM_011522427.1:c.641A>C	XP_011520729.1:p.Asp214Ala
XR_932805.1:n.2150A>C
XM_011522424.3:c.2129A>C	XP_011520726.1:p.Asp710Ala
XM_017023043.2:c.1202A>C	XP_016878532.1:p.Asp401Ala
NM_005236.3:c.1991A>C MANE Select	NP_005227.1:p.Asp664Ala