Canonical Allele Identifier: CA2575929531
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs2141619537

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947531A>T , CM000678.2:g.13947531A>T GRCh38
NC_000016.9:g.14041388A>T , CM000678.1:g.14041388A>T GRCh37
NC_000016.8:g.13948889A>T NCBI36
NG_011442.1:g.32375A>T , LRG_463:g.32375A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2156-83A>T ENSP00000507912.1:n.2156-83A>T
ENST00000683962.1:c.*1712-83A>T ENSP00000506854.1:n.*1712-83A>T
ENST00000311895.8:c.2018-83A>T MANE Select ENSP00000310520.7:n.2018-83A>T
ENST00000311895.7:c.2018-83A>T ENSP00000310520.7:n.2018-83A>T
ENST00000389138.7:n.1295-83A>T
ENST00000462862.1:c.331-83A>T ENSP00000461322.1:n.331-83A>T
NM_005236.2:c.2018-83A>T , LRG_463t1:c.2018-83A>T NP_005227.1:n.2018-83A>T
XM_011522424.1:c.2156-83A>T XP_011520726.1:n.2156-83A>T
XM_011522425.1:c.1475-83A>T XP_011520727.1:n.1475-83A>T
XM_011522426.1:c.1229-83A>T XP_011520728.1:n.1229-83A>T
XM_011522427.1:c.668-83A>T XP_011520729.1:n.668-83A>T
XR_932805.1:n.2177-83A>T
XM_011522424.3:c.2156-83A>T XP_011520726.1:n.2156-83A>T
XM_017023043.2:c.1229-83A>T XP_016878532.1:n.1229-83A>T
NM_005236.3:c.2018-83A>T MANE Select NP_005227.1:n.2018-83A>T