Canonical Allele Identifier: CA2160045324

Gene: TRAF3

Genomic Alleles

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

Transcript Alleles

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