Canonical Allele Identifier: CA394824310
Gene: ERCC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.14041979G>T (hg19) chr16:g.13948122G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948122G>T , CM000678.2:g.13948122G>T GRCh38
NC_000016.9:g.14041979G>T , CM000678.1:g.14041979G>T GRCh37
NC_000016.8:g.13949480G>T NCBI36
NG_011442.1:g.32966G>T , LRG_463:g.32966G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2664G>T ENSP00000507912.1:p.Glu888Asp
ENST00000683962.1:c.*2220G>T ENSP00000506854.1:n.*2220G>T
ENST00000311895.8:c.2526G>T MANE Select ENSP00000310520.7:p.Glu842Asp
ENST00000311895.7:c.2526G>T ENSP00000310520.7:p.Glu842Asp
ENST00000389138.7:n.1803G>T
NM_005236.2:c.2526G>T , LRG_463t1:c.2526G>T NP_005227.1:p.Glu842Asp
XM_011522424.1:c.2664G>T XP_011520726.1:p.Glu888Asp
XM_011522425.1:c.1983G>T XP_011520727.1:p.Glu661Asp
XM_011522426.1:c.1737G>T XP_011520728.1:p.Glu579Asp
XM_011522427.1:c.1176G>T XP_011520729.1:p.Glu392Asp
XR_932805.1:n.2685G>T
XM_011522424.3:c.2664G>T XP_011520726.1:p.Glu888Asp
XM_017023043.2:c.1737G>T XP_016878532.1:p.Glu579Asp
NM_005236.3:c.2526G>T MANE Select NP_005227.1:p.Glu842Asp
Search 100 bp 5'
Search 100 bp 3'