Canonical Allele Identifier: CA394812826

Gene: ERCC4

Linked Data

• dbSNP Id: rs753641687
• gnomAD v4: 16-13935728-C-G
• MyVariant Identifiers: chr16:g.14029585C>G (hg19) ; chr16:g.13935728C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935728C>G , CM000678.2:g.13935728C>G	GRCh38
NC_000016.9:g.14029585C>G , CM000678.1:g.14029585C>G	GRCh37
NC_000016.8:g.13937086C>G	NCBI36
NG_011442.1:g.20572C>G , LRG_463:g.20572C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1874C>G
ENST00000682617.1:c.1934C>G	ENSP00000507912.1:p.Pro645Arg
ENST00000682826.1:c.*1110C>G	ENSP00000507274.1:n.*1110C>G
ENST00000682909.1:n.3836C>G
ENST00000683277.1:n.3441C>G
ENST00000683407.1:n.1804C>G
ENST00000683962.1:c.*1490C>G	ENSP00000506854.1:n.*1490C>G
ENST00000311895.8:c.1796C>G MANE Select	ENSP00000310520.7:p.Pro599Arg
ENST00000311895.7:c.1796C>G	ENSP00000310520.7:p.Pro599Arg
ENST00000389138.7:n.1073C>G
NM_005236.2:c.1796C>G , LRG_463t1:c.1796C>G	NP_005227.1:p.Pro599Arg
XM_011522424.1:c.1934C>G	XP_011520726.1:p.Pro645Arg
XM_011522425.1:c.1253C>G	XP_011520727.1:p.Pro418Arg
XM_011522426.1:c.1007C>G	XP_011520728.1:p.Pro336Arg
XM_011522427.1:c.446C>G	XP_011520729.1:p.Pro149Arg
XR_932805.1:n.1955C>G
XM_011522424.3:c.1934C>G	XP_011520726.1:p.Pro645Arg
XM_017023043.2:c.1007C>G	XP_016878532.1:p.Pro336Arg
NM_005236.3:c.1796C>G MANE Select	NP_005227.1:p.Pro599Arg