Canonical Allele Identifier: CA394821805

Gene: ERCC4

Linked Data

• dbSNP Id: rs774900622
• gnomAD v4: 16-13947704-G-A
• MyVariant Identifiers: chr16:g.14041561G>A (hg19) ; chr16:g.13947704G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947704G>A , CM000678.2:g.13947704G>A	GRCh38
NC_000016.9:g.14041561G>A , CM000678.1:g.14041561G>A	GRCh37
NC_000016.8:g.13949062G>A	NCBI36
NG_011442.1:g.32548G>A , LRG_463:g.32548G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2246G>A	ENSP00000507912.1:p.Gly749Asp
ENST00000683962.1:c.*1802G>A	ENSP00000506854.1:n.*1802G>A
ENST00000311895.8:c.2108G>A MANE Select	ENSP00000310520.7:p.Gly703Asp
ENST00000311895.7:c.2108G>A	ENSP00000310520.7:p.Gly703Asp
ENST00000389138.7:n.1385G>A
ENST00000462862.1:c.421G>A	ENSP00000461322.1:n.421G>A
NM_005236.2:c.2108G>A , LRG_463t1:c.2108G>A	NP_005227.1:p.Gly703Asp
XM_011522424.1:c.2246G>A	XP_011520726.1:p.Gly749Asp
XM_011522425.1:c.1565G>A	XP_011520727.1:p.Gly522Asp
XM_011522426.1:c.1319G>A	XP_011520728.1:p.Gly440Asp
XM_011522427.1:c.758G>A	XP_011520729.1:p.Gly253Asp
XR_932805.1:n.2267G>A
XM_011522424.3:c.2246G>A	XP_011520726.1:p.Gly749Asp
XM_017023043.2:c.1319G>A	XP_016878532.1:p.Gly440Asp
NM_005236.3:c.2108G>A MANE Select	NP_005227.1:p.Gly703Asp