Canonical Allele Identifier: CA394824474

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141621129
• MyVariant Identifiers: chr16:g.14042020C>G (hg19) ; chr16:g.13948163C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948163C>G , CM000678.2:g.13948163C>G	GRCh38
NC_000016.9:g.14042020C>G , CM000678.1:g.14042020C>G	GRCh37
NC_000016.8:g.13949521C>G	NCBI36
NG_011442.1:g.33007C>G , LRG_463:g.33007C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2705C>G	ENSP00000507912.1:p.Pro902Arg
ENST00000683962.1:c.*2261C>G	ENSP00000506854.1:n.*2261C>G
ENST00000311895.8:c.2567C>G MANE Select	ENSP00000310520.7:p.Pro856Arg
ENST00000311895.7:c.2567C>G	ENSP00000310520.7:p.Pro856Arg
ENST00000389138.7:n.1844C>G
NM_005236.2:c.2567C>G , LRG_463t1:c.2567C>G	NP_005227.1:p.Pro856Arg
XM_011522424.1:c.2705C>G	XP_011520726.1:p.Pro902Arg
XM_011522425.1:c.2024C>G	XP_011520727.1:p.Pro675Arg
XM_011522426.1:c.1778C>G	XP_011520728.1:p.Pro593Arg
XM_011522427.1:c.1217C>G	XP_011520729.1:p.Pro406Arg
XR_932805.1:n.2726C>G
XM_011522424.3:c.2705C>G	XP_011520726.1:p.Pro902Arg
XM_017023043.2:c.1778C>G	XP_016878532.1:p.Pro593Arg
NM_005236.3:c.2567C>G MANE Select	NP_005227.1:p.Pro856Arg