Canonical Allele Identifier: CA394822914
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947896T>G , CM000678.2:g.13947896T>G GRCh38
NC_000016.9:g.14041753T>G , CM000678.1:g.14041753T>G GRCh37
NC_000016.8:g.13949254T>G NCBI36
NG_011442.1:g.32740T>G , LRG_463:g.32740T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2438T>G ENSP00000507912.1:p.Phe813Cys
ENST00000683962.1:c.*1994T>G ENSP00000506854.1:n.*1994T>G
ENST00000311895.8:c.2300T>G MANE Select ENSP00000310520.7:p.Phe767Cys
ENST00000311895.7:c.2300T>G ENSP00000310520.7:p.Phe767Cys
ENST00000389138.7:n.1577T>G
ENST00000462862.1:c.613T>G ENSP00000461322.1:n.613T>G
NM_005236.2:c.2300T>G , LRG_463t1:c.2300T>G NP_005227.1:p.Phe767Cys
XM_011522424.1:c.2438T>G XP_011520726.1:p.Phe813Cys
XM_011522425.1:c.1757T>G XP_011520727.1:p.Phe586Cys
XM_011522426.1:c.1511T>G XP_011520728.1:p.Phe504Cys
XM_011522427.1:c.950T>G XP_011520729.1:p.Phe317Cys
XR_932805.1:n.2459T>G
XM_011522424.3:c.2438T>G XP_011520726.1:p.Phe813Cys
XM_017023043.2:c.1511T>G XP_016878532.1:p.Phe504Cys
NM_005236.3:c.2300T>G MANE Select NP_005227.1:p.Phe767Cys