Canonical Allele Identifier: CA278486151

Gene: ERCC4

Linked Data

• dbSNP Id: rs916059697
• MyVariant Identifiers: chr16:g.14042224T>G (hg19) ; chr16:g.13948367T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948367T>G , CM000678.2:g.13948367T>G	GRCh38
NC_000016.9:g.14042224T>G , CM000678.1:g.14042224T>G	GRCh37
NC_000016.8:g.13949725T>G	NCBI36
NG_011442.1:g.33211T>G , LRG_463:g.33211T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*20T>G	ENSP00000507912.1:n.*20T>G
ENST00000683962.1:c.*2465T>G	ENSP00000506854.1:n.*2465T>G
ENST00000311895.8:c.*20T>G MANE Select	ENSP00000310520.7:n.*20T>G
ENST00000311895.7:c.*20T>G	ENSP00000310520.7:n.*20T>G
ENST00000389138.7:n.2048T>G
NM_005236.2:c.*20T>G , LRG_463t1:c.*20T>G	NP_005227.1:n.*20T>G
XM_011522424.1:c.*20T>G	XP_011520726.1:n.*20T>G
XM_011522425.1:c.*20T>G	XP_011520727.1:n.*20T>G
XM_011522426.1:c.*20T>G	XP_011520728.1:n.*20T>G
XM_011522427.1:c.*20T>G	XP_011520729.1:n.*20T>G
XR_932805.1:n.2930T>G
XM_011522424.3:c.*20T>G	XP_011520726.1:n.*20T>G
XM_017023043.2:c.*20T>G	XP_016878532.1:n.*20T>G
NM_005236.3:c.*20T>G MANE Select	NP_005227.1:n.*20T>G