Canonical Allele Identifier: CA14017347
Gene: TRAF3 HGNC NCBI

Linked Data

dbSNP Id: rs10133111

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102910984G>A , CM000676.2:g.102910984G>A GRCh38
NC_000014.8:g.103377321G>A , CM000676.1:g.103377321G>A GRCh37
NC_000014.7:g.102447074G>A NCBI36
NG_027973.1:g.138506G>A , LRG_229:g.138506G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000351691.10:c.*5200G>A ENSP00000332468.5:n.*5200G>A
ENST00000699893.1:c.*5200G>A ENSP00000514677.1:n.*5200G>A
ENST00000699894.1:c.*5200G>A ENSP00000514678.1:n.*5200G>A
ENST00000699895.1:n.6956G>A
ENST00000699896.1:n.1067-146G>A
ENST00000699897.1:n.8984G>A
ENST00000392745.8:c.*5200G>A MANE Select ENSP00000376500.3:n.*5200G>A
ENST00000347662.8:c.*5200G>A ENSP00000328003.4:n.*5200G>A
ENST00000560371.5:c.*5200G>A ENSP00000454207.1:n.*5200G>A
NM_001199427.1:c.*5200G>A NP_001186356.1:n.*5200G>A
NM_003300.3:c.*5200G>A NP_003291.2:n.*5200G>A
NM_145725.2:c.*5200G>A , LRG_229t1:c.*5200G>A NP_663777.1:n.*5200G>A
NM_145726.2:c.*5200G>A NP_663778.1:n.*5200G>A
XM_011537116.1:c.*5200G>A XP_011535418.1:n.*5200G>A
XM_011537117.1:c.*5200G>A XP_011535419.1:n.*5200G>A
XM_011537118.1:c.*5200G>A XP_011535420.1:n.*5200G>A
XM_011537116.3:c.*5200G>A XP_011535418.1:n.*5200G>A
XM_011537117.3:c.*5200G>A XP_011535419.1:n.*5200G>A
XM_011537118.3:c.*5200G>A XP_011535420.1:n.*5200G>A
XM_017021617.1:c.*5200G>A XP_016877106.1:n.*5200G>A
XM_017021618.1:c.*5200G>A XP_016877107.1:n.*5200G>A
XM_017021619.1:c.*5200G>A XP_016877108.1:n.*5200G>A
NM_001199427.2:c.*5200G>A NP_001186356.1:n.*5200G>A
NM_003300.4:c.*5200G>A NP_003291.2:n.*5200G>A
NM_145725.3:c.*5200G>A MANE Select NP_663777.1:n.*5200G>A
NM_001385142.1:c.*5200G>A NP_001372071.1:n.*5200G>A
NM_001385143.1:c.*5200G>A NP_001372072.1:n.*5200G>A
NM_145726.3:c.*5200G>A NP_663778.1:n.*5200G>A