Canonical Allele Identifier: CA2209082975
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948334A= , CM000678.2:g.13948334A= GRCh38
NC_000016.9:g.14042191A= , CM000678.1:g.14042191A= GRCh37
NC_000016.8:g.13949692A= NCBI36
NG_011442.1:g.33178A= , LRG_463:g.33178A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2876A= ENSP00000507912.1:p.Lys959=
ENST00000683962.1:c.*2432A= ENSP00000506854.1:n.*2432A=
ENST00000311895.8:c.2738A= MANE Select ENSP00000310520.7:p.Lys913=
ENST00000311895.7:c.2738A= ENSP00000310520.7:p.Lys913=
ENST00000389138.7:n.2015A=
NM_005236.2:c.2738A= , LRG_463t1:c.2738A= NP_005227.1:p.Lys913=
XM_011522424.1:c.2876A= XP_011520726.1:p.Lys959=
XM_011522425.1:c.2195A= XP_011520727.1:p.Lys732=
XM_011522426.1:c.1949A= XP_011520728.1:p.Lys650=
XM_011522427.1:c.1388A= XP_011520729.1:p.Lys463=
XR_932805.1:n.2897A=
XM_011522424.3:c.2876A= XP_011520726.1:p.Lys959=
XM_017023043.2:c.1949A= XP_016878532.1:p.Lys650=
NM_005236.3:c.2738A= MANE Select NP_005227.1:p.Lys913=