Canonical Allele Identifier: CA394822920
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs2032550570

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947897C>G , CM000678.2:g.13947897C>G GRCh38
NC_000016.9:g.14041754C>G , CM000678.1:g.14041754C>G GRCh37
NC_000016.8:g.13949255C>G NCBI36
NG_011442.1:g.32741C>G , LRG_463:g.32741C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2439C>G ENSP00000507912.1:p.Phe813Leu
ENST00000683962.1:c.*1995C>G ENSP00000506854.1:n.*1995C>G
ENST00000311895.8:c.2301C>G MANE Select ENSP00000310520.7:p.Phe767Leu
ENST00000311895.7:c.2301C>G ENSP00000310520.7:p.Phe767Leu
ENST00000389138.7:n.1578C>G
ENST00000462862.1:c.614C>G ENSP00000461322.1:n.614C>G
NM_005236.2:c.2301C>G , LRG_463t1:c.2301C>G NP_005227.1:p.Phe767Leu
XM_011522424.1:c.2439C>G XP_011520726.1:p.Phe813Leu
XM_011522425.1:c.1758C>G XP_011520727.1:p.Phe586Leu
XM_011522426.1:c.1512C>G XP_011520728.1:p.Phe504Leu
XM_011522427.1:c.951C>G XP_011520729.1:p.Phe317Leu
XR_932805.1:n.2460C>G
XM_011522424.3:c.2439C>G XP_011520726.1:p.Phe813Leu
XM_017023043.2:c.1512C>G XP_016878532.1:p.Phe504Leu
NM_005236.3:c.2301C>G MANE Select NP_005227.1:p.Phe767Leu