Canonical Allele Identifier: CA7910735
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs769080259

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2564C>T ENSP00000507912.1:p.Thr855Met
ENST00000683962.1:c.*2120C>T ENSP00000506854.1:n.*2120C>T
ENST00000311895.8:c.2426C>T MANE Select ENSP00000310520.7:p.Thr809Met
ENST00000311895.7:c.2426C>T ENSP00000310520.7:p.Thr809Met
ENST00000389138.7:n.1703C>T
NM_005236.2:c.2426C>T , LRG_463t1:c.2426C>T NP_005227.1:p.Thr809Met
XM_011522424.1:c.2564C>T XP_011520726.1:p.Thr855Met
XM_011522425.1:c.1883C>T XP_011520727.1:p.Thr628Met
XM_011522426.1:c.1637C>T XP_011520728.1:p.Thr546Met
XM_011522427.1:c.1076C>T XP_011520729.1:p.Thr359Met
XR_932805.1:n.2585C>T
XM_011522424.3:c.2564C>T XP_011520726.1:p.Thr855Met
XM_017023043.2:c.1637C>T XP_016878532.1:p.Thr546Met
NM_005236.3:c.2426C>T MANE Select NP_005227.1:p.Thr809Met