Canonical Allele Identifier: CA7910727
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs763726880

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947957A>G , CM000678.2:g.13947957A>G GRCh38
NC_000016.9:g.14041814A>G , CM000678.1:g.14041814A>G GRCh37
NC_000016.8:g.13949315A>G NCBI36
NG_011442.1:g.32801A>G , LRG_463:g.32801A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2499A>G ENSP00000507912.1:p.Lys833=
ENST00000683962.1:c.*2055A>G ENSP00000506854.1:n.*2055A>G
ENST00000311895.8:c.2361A>G MANE Select ENSP00000310520.7:p.Lys787=
ENST00000311895.7:c.2361A>G ENSP00000310520.7:p.Lys787=
ENST00000389138.7:n.1638A>G
ENST00000462862.1:c.674A>G ENSP00000461322.1:n.674A>G
NM_005236.2:c.2361A>G , LRG_463t1:c.2361A>G NP_005227.1:p.Lys787=
XM_011522424.1:c.2499A>G XP_011520726.1:p.Lys833=
XM_011522425.1:c.1818A>G XP_011520727.1:p.Lys606=
XM_011522426.1:c.1572A>G XP_011520728.1:p.Lys524=
XM_011522427.1:c.1011A>G XP_011520729.1:p.Lys337=
XR_932805.1:n.2520A>G
XM_011522424.3:c.2499A>G XP_011520726.1:p.Lys833=
XM_017023043.2:c.1572A>G XP_016878532.1:p.Lys524=
NM_005236.3:c.2361A>G MANE Select NP_005227.1:p.Lys787=