Canonical Allele Identifier: CA394812459

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029485C>A (hg19) ; chr16:g.13935628C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935628C>A , CM000678.2:g.13935628C>A	GRCh38
NC_000016.9:g.14029485C>A , CM000678.1:g.14029485C>A	GRCh37
NC_000016.8:g.13936986C>A	NCBI36
NG_011442.1:g.20472C>A , LRG_463:g.20472C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1774C>A
ENST00000682617.1:c.1834C>A	ENSP00000507912.1:p.Leu612Met
ENST00000682826.1:c.*1010C>A	ENSP00000507274.1:n.*1010C>A
ENST00000682909.1:n.3736C>A
ENST00000683277.1:n.3341C>A
ENST00000683407.1:n.1704C>A
ENST00000683962.1:c.*1390C>A	ENSP00000506854.1:n.*1390C>A
ENST00000311895.8:c.1696C>A MANE Select	ENSP00000310520.7:p.Leu566Met
ENST00000311895.7:c.1696C>A	ENSP00000310520.7:p.Leu566Met
ENST00000389138.7:n.973C>A
NM_005236.2:c.1696C>A , LRG_463t1:c.1696C>A	NP_005227.1:p.Leu566Met
XM_011522424.1:c.1834C>A	XP_011520726.1:p.Leu612Met
XM_011522425.1:c.1153C>A	XP_011520727.1:p.Leu385Met
XM_011522426.1:c.907C>A	XP_011520728.1:p.Leu303Met
XM_011522427.1:c.346C>A	XP_011520729.1:p.Leu116Met
XR_932805.1:n.1855C>A
XM_011522424.3:c.1834C>A	XP_011520726.1:p.Leu612Met
XM_017023043.2:c.907C>A	XP_016878532.1:p.Leu303Met
NM_005236.3:c.1696C>A MANE Select	NP_005227.1:p.Leu566Met