Canonical Allele Identifier: CA493690022

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13947969-T-G
• MyVariant Identifiers: chr16:g.14041826T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947969T>G , CM000678.2:g.13947969T>G	GRCh38
NC_000016.9:g.14041826T>G , CM000678.1:g.14041826T>G	GRCh37
NC_000016.8:g.13949327T>G	NCBI36
NG_011442.1:g.32813T>G , LRG_463:g.32813T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2511T>G	ENSP00000507912.1:p.Leu837=
ENST00000683962.1:c.*2067T>G	ENSP00000506854.1:n.*2067T>G
ENST00000311895.8:c.2373T>G MANE Select	ENSP00000310520.7:p.Leu791=
ENST00000311895.7:c.2373T>G	ENSP00000310520.7:p.Leu791=
ENST00000389138.7:n.1650T>G
ENST00000462862.1:c.686T>G	ENSP00000461322.1:n.686T>G
NM_005236.2:c.2373T>G , LRG_463t1:c.2373T>G	NP_005227.1:p.Leu791=
XM_011522424.1:c.2511T>G	XP_011520726.1:p.Leu837=
XM_011522425.1:c.1830T>G	XP_011520727.1:p.Leu610=
XM_011522426.1:c.1584T>G	XP_011520728.1:p.Leu528=
XM_011522427.1:c.1023T>G	XP_011520729.1:p.Leu341=
XR_932805.1:n.2532T>G
XM_011522424.3:c.2511T>G	XP_011520726.1:p.Leu837=
XM_017023043.2:c.1584T>G	XP_016878532.1:p.Leu528=
NM_005236.3:c.2373T>G MANE Select	NP_005227.1:p.Leu791=