Canonical Allele Identifier: CA394823449
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947996T>G , CM000678.2:g.13947996T>G GRCh38
NC_000016.9:g.14041853T>G , CM000678.1:g.14041853T>G GRCh37
NC_000016.8:g.13949354T>G NCBI36
NG_011442.1:g.32840T>G , LRG_463:g.32840T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2538T>G ENSP00000507912.1:p.Ile846Met
ENST00000683962.1:c.*2094T>G ENSP00000506854.1:n.*2094T>G
ENST00000311895.8:c.2400T>G MANE Select ENSP00000310520.7:p.Ile800Met
ENST00000311895.7:c.2400T>G ENSP00000310520.7:p.Ile800Met
ENST00000389138.7:n.1677T>G
ENST00000462862.1:c.713T>G ENSP00000461322.1:n.713T>G
NM_005236.2:c.2400T>G , LRG_463t1:c.2400T>G NP_005227.1:p.Ile800Met
XM_011522424.1:c.2538T>G XP_011520726.1:p.Ile846Met
XM_011522425.1:c.1857T>G XP_011520727.1:p.Ile619Met
XM_011522426.1:c.1611T>G XP_011520728.1:p.Ile537Met
XM_011522427.1:c.1050T>G XP_011520729.1:p.Ile350Met
XR_932805.1:n.2559T>G
XM_011522424.3:c.2538T>G XP_011520726.1:p.Ile846Met
XM_017023043.2:c.1611T>G XP_016878532.1:p.Ile537Met
NM_005236.3:c.2400T>G MANE Select NP_005227.1:p.Ile800Met