Canonical Allele Identifier: CA7910677
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs772728961

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947697C>G , CM000678.2:g.13947697C>G GRCh38
NC_000016.9:g.14041554C>G , CM000678.1:g.14041554C>G GRCh37
NC_000016.8:g.13949055C>G NCBI36
NG_011442.1:g.32541C>G , LRG_463:g.32541C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2239C>G ENSP00000507912.1:p.Arg747Gly
ENST00000683962.1:c.*1795C>G ENSP00000506854.1:n.*1795C>G
ENST00000311895.8:c.2101C>G MANE Select ENSP00000310520.7:p.Arg701Gly
ENST00000311895.7:c.2101C>G ENSP00000310520.7:p.Arg701Gly
ENST00000389138.7:n.1378C>G
ENST00000462862.1:c.414C>G ENSP00000461322.1:n.414C>G
NM_005236.2:c.2101C>G , LRG_463t1:c.2101C>G NP_005227.1:p.Arg701Gly
XM_011522424.1:c.2239C>G XP_011520726.1:p.Arg747Gly
XM_011522425.1:c.1558C>G XP_011520727.1:p.Arg520Gly
XM_011522426.1:c.1312C>G XP_011520728.1:p.Arg438Gly
XM_011522427.1:c.751C>G XP_011520729.1:p.Arg251Gly
XR_932805.1:n.2260C>G
XM_011522424.3:c.2239C>G XP_011520726.1:p.Arg747Gly
XM_017023043.2:c.1312C>G XP_016878532.1:p.Arg438Gly
NM_005236.3:c.2101C>G MANE Select NP_005227.1:p.Arg701Gly