Canonical Allele Identifier: CA394822706

Gene: ERCC4

Linked Data

• ClinVar Variation Id: 2171834
• ClinVar RCV Id: RCV003097446
• gnomAD v4: 16-13947848-A-G
• MyVariant Identifiers: chr16:g.14041705A>G (hg19) ; chr16:g.13947848A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947848A>G , CM000678.2:g.13947848A>G	GRCh38
NC_000016.9:g.14041705A>G , CM000678.1:g.14041705A>G	GRCh37
NC_000016.8:g.13949206A>G	NCBI36
NG_011442.1:g.32692A>G , LRG_463:g.32692A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2390A>G	ENSP00000507912.1:p.Tyr797Cys
ENST00000683962.1:c.*1946A>G	ENSP00000506854.1:n.*1946A>G
ENST00000311895.8:c.2252A>G MANE Select	ENSP00000310520.7:p.Tyr751Cys
ENST00000311895.7:c.2252A>G	ENSP00000310520.7:p.Tyr751Cys
ENST00000389138.7:n.1529A>G
ENST00000462862.1:c.565A>G	ENSP00000461322.1:n.565A>G
NM_005236.2:c.2252A>G , LRG_463t1:c.2252A>G	NP_005227.1:p.Tyr751Cys
XM_011522424.1:c.2390A>G	XP_011520726.1:p.Tyr797Cys
XM_011522425.1:c.1709A>G	XP_011520727.1:p.Tyr570Cys
XM_011522426.1:c.1463A>G	XP_011520728.1:p.Tyr488Cys
XM_011522427.1:c.902A>G	XP_011520729.1:p.Tyr301Cys
XR_932805.1:n.2411A>G
XM_011522424.3:c.2390A>G	XP_011520726.1:p.Tyr797Cys
XM_017023043.2:c.1463A>G	XP_016878532.1:p.Tyr488Cys
NM_005236.3:c.2252A>G MANE Select	NP_005227.1:p.Tyr751Cys