Canonical Allele Identifier: CA394824431

Gene: ERCC4

Linked Data

• dbSNP Id: rs2032559019
• MyVariant Identifiers: chr16:g.14042003C>A (hg19) ; chr16:g.13948146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948146C>A , CM000678.2:g.13948146C>A	GRCh38
NC_000016.9:g.14042003C>A , CM000678.1:g.14042003C>A	GRCh37
NC_000016.8:g.13949504C>A	NCBI36
NG_011442.1:g.32990C>A , LRG_463:g.32990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2688C>A	ENSP00000507912.1:p.Asp896Glu
ENST00000683962.1:c.*2244C>A	ENSP00000506854.1:n.*2244C>A
ENST00000311895.8:c.2550C>A MANE Select	ENSP00000310520.7:p.Asp850Glu
ENST00000311895.7:c.2550C>A	ENSP00000310520.7:p.Asp850Glu
ENST00000389138.7:n.1827C>A
NM_005236.2:c.2550C>A , LRG_463t1:c.2550C>A	NP_005227.1:p.Asp850Glu
XM_011522424.1:c.2688C>A	XP_011520726.1:p.Asp896Glu
XM_011522425.1:c.2007C>A	XP_011520727.1:p.Asp669Glu
XM_011522426.1:c.1761C>A	XP_011520728.1:p.Asp587Glu
XM_011522427.1:c.1200C>A	XP_011520729.1:p.Asp400Glu
XR_932805.1:n.2709C>A
XM_011522424.3:c.2688C>A	XP_011520726.1:p.Asp896Glu
XM_017023043.2:c.1761C>A	XP_016878532.1:p.Asp587Glu
NM_005236.3:c.2550C>A MANE Select	NP_005227.1:p.Asp850Glu