Canonical Allele Identifier: CA7359237
Gene: TRAF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1168583
ClinVar RCV Id: RCV001518952
dbSNP Id: rs1131877

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102875712T>C , CM000676.2:g.102875712T>C GRCh38
NC_000014.8:g.103342049T>C , CM000676.1:g.103342049T>C GRCh37
NC_000014.7:g.102411802T>C NCBI36
NG_027973.1:g.103234T>C , LRG_229:g.103234T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351691.10:c.386T>C ENSP00000332468.5:p.Met129Thr
ENST00000699893.1:c.386T>C ENSP00000514677.1:p.Met129Thr
ENST00000699894.1:c.386T>C ENSP00000514678.1:p.Met129Thr
ENST00000699895.1:n.516T>C
ENST00000699896.1:n.317T>C
ENST00000392745.8:c.386T>C MANE Select ENSP00000376500.3:p.Met129Thr
ENST00000347662.8:c.386T>C ENSP00000328003.4:p.Met129Thr
ENST00000351691.9:c.386T>C ENSP00000332468.5:p.Met129Thr
ENST00000392745.6:c.386T>C ENSP00000376500.2:p.Met129Thr
ENST00000539721.5:c.386T>C ENSP00000445998.1:p.Met129Thr
ENST00000558700.5:c.131T>C ENSP00000453031.1:p.Met44Thr
ENST00000558880.1:n.38T>C
ENST00000559734.1:c.26T>C ENSP00000453032.1:p.Met9Thr
ENST00000560371.5:c.386T>C ENSP00000454207.1:p.Met129Thr
NM_001199427.1:c.386T>C NP_001186356.1:p.Met129Thr
NM_003300.3:c.386T>C NP_003291.2:p.Met129Thr
NM_145725.2:c.386T>C , LRG_229t1:c.386T>C NP_663777.1:p.Met129Thr
NM_145726.2:c.386T>C NP_663778.1:p.Met129Thr
XM_011537116.1:c.386T>C XP_011535418.1:p.Met129Thr
XM_011537117.1:c.386T>C XP_011535419.1:p.Met129Thr
XM_011537118.1:c.386T>C XP_011535420.1:p.Met129Thr
XR_943512.1:n.743T>C
XM_011537116.3:c.386T>C XP_011535418.1:p.Met129Thr
XM_011537117.3:c.386T>C XP_011535419.1:p.Met129Thr
XM_011537118.3:c.386T>C XP_011535420.1:p.Met129Thr
XM_017021617.1:c.386T>C XP_016877106.1:p.Met129Thr
XM_017021618.1:c.386T>C XP_016877107.1:p.Met129Thr
XM_017021619.1:c.386T>C XP_016877108.1:p.Met129Thr
XM_017021620.2:c.386T>C XP_016877109.1:p.Met129Thr
NM_001199427.2:c.386T>C NP_001186356.1:p.Met129Thr
NM_003300.4:c.386T>C NP_003291.2:p.Met129Thr
NM_145725.3:c.386T>C MANE Select NP_663777.1:p.Met129Thr
NM_001385142.1:c.386T>C NP_001372071.1:p.Met129Thr
NM_001385143.1:c.386T>C NP_001372072.1:p.Met129Thr
NM_145726.3:c.386T>C NP_663778.1:p.Met129Thr