Canonical Allele Identifier: CA493689646

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141619878
• MyVariant Identifiers: chr16:g.14041568C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947711C>T , CM000678.2:g.13947711C>T	GRCh38
NC_000016.9:g.14041568C>T , CM000678.1:g.14041568C>T	GRCh37
NC_000016.8:g.13949069C>T	NCBI36
NG_011442.1:g.32555C>T , LRG_463:g.32555C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2253C>T	ENSP00000507912.1:p.Asp751=
ENST00000683962.1:c.*1809C>T	ENSP00000506854.1:n.*1809C>T
ENST00000311895.8:c.2115C>T MANE Select	ENSP00000310520.7:p.Asp705=
ENST00000311895.7:c.2115C>T	ENSP00000310520.7:p.Asp705=
ENST00000389138.7:n.1392C>T
ENST00000462862.1:c.428C>T	ENSP00000461322.1:n.428C>T
NM_005236.2:c.2115C>T , LRG_463t1:c.2115C>T	NP_005227.1:p.Asp705=
XM_011522424.1:c.2253C>T	XP_011520726.1:p.Asp751=
XM_011522425.1:c.1572C>T	XP_011520727.1:p.Asp524=
XM_011522426.1:c.1326C>T	XP_011520728.1:p.Asp442=
XM_011522427.1:c.765C>T	XP_011520729.1:p.Asp255=
XR_932805.1:n.2274C>T
XM_011522424.3:c.2253C>T	XP_011520726.1:p.Asp751=
XM_017023043.2:c.1326C>T	XP_016878532.1:p.Asp442=
NM_005236.3:c.2115C>T MANE Select	NP_005227.1:p.Asp705=