Canonical Allele Identifier: CA394823676
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948022C>G , CM000678.2:g.13948022C>G GRCh38
NC_000016.9:g.14041879C>G , CM000678.1:g.14041879C>G GRCh37
NC_000016.8:g.13949380C>G NCBI36
NG_011442.1:g.32866C>G , LRG_463:g.32866C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2564C>G ENSP00000507912.1:p.Thr855Arg
ENST00000683962.1:c.*2120C>G ENSP00000506854.1:n.*2120C>G
ENST00000311895.8:c.2426C>G MANE Select ENSP00000310520.7:p.Thr809Arg
ENST00000311895.7:c.2426C>G ENSP00000310520.7:p.Thr809Arg
ENST00000389138.7:n.1703C>G
NM_005236.2:c.2426C>G , LRG_463t1:c.2426C>G NP_005227.1:p.Thr809Arg
XM_011522424.1:c.2564C>G XP_011520726.1:p.Thr855Arg
XM_011522425.1:c.1883C>G XP_011520727.1:p.Thr628Arg
XM_011522426.1:c.1637C>G XP_011520728.1:p.Thr546Arg
XM_011522427.1:c.1076C>G XP_011520729.1:p.Thr359Arg
XR_932805.1:n.2585C>G
XM_011522424.3:c.2564C>G XP_011520726.1:p.Thr855Arg
XM_017023043.2:c.1637C>G XP_016878532.1:p.Thr546Arg
NM_005236.3:c.2426C>G MANE Select NP_005227.1:p.Thr809Arg