Canonical Allele Identifier: CA394812419

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13935620-C-A
• MyVariant Identifiers: chr16:g.14029477C>A (hg19) ; chr16:g.13935620C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935620C>A , CM000678.2:g.13935620C>A	GRCh38
NC_000016.9:g.14029477C>A , CM000678.1:g.14029477C>A	GRCh37
NC_000016.8:g.13936978C>A	NCBI36
NG_011442.1:g.20464C>A , LRG_463:g.20464C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1766C>A
ENST00000682617.1:c.1826C>A	ENSP00000507912.1:p.Pro609His
ENST00000682826.1:c.*1002C>A	ENSP00000507274.1:n.*1002C>A
ENST00000682909.1:n.3728C>A
ENST00000683277.1:n.3333C>A
ENST00000683407.1:n.1696C>A
ENST00000683962.1:c.*1382C>A	ENSP00000506854.1:n.*1382C>A
ENST00000311895.8:c.1688C>A MANE Select	ENSP00000310520.7:p.Pro563His
ENST00000311895.7:c.1688C>A	ENSP00000310520.7:p.Pro563His
ENST00000389138.7:n.965C>A
NM_005236.2:c.1688C>A , LRG_463t1:c.1688C>A	NP_005227.1:p.Pro563His
XM_011522424.1:c.1826C>A	XP_011520726.1:p.Pro609His
XM_011522425.1:c.1145C>A	XP_011520727.1:p.Pro382His
XM_011522426.1:c.899C>A	XP_011520728.1:p.Pro300His
XM_011522427.1:c.338C>A	XP_011520729.1:p.Pro113His
XR_932805.1:n.1847C>A
XM_011522424.3:c.1826C>A	XP_011520726.1:p.Pro609His
XM_017023043.2:c.899C>A	XP_016878532.1:p.Pro300His
NM_005236.3:c.1688C>A MANE Select	NP_005227.1:p.Pro563His