Canonical Allele Identifier: CA391076786

Gene: TRAF3

Linked Data

• MyVariant Identifiers: chr14:g.103371824C>G (hg19) ; chr14:g.102905487C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102905487C>G , CM000676.2:g.102905487C>G	GRCh38
NC_000014.8:g.103371824C>G , CM000676.1:g.103371824C>G	GRCh37
NC_000014.7:g.102441577C>G	NCBI36
NG_027973.1:g.133009C>G , LRG_229:g.133009C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000351691.10:c.1335C>G	ENSP00000332468.5:p.His445Gln
ENST00000699893.1:c.1335C>G	ENSP00000514677.1:p.His445Gln
ENST00000699894.1:c.1410C>G	ENSP00000514678.1:p.His470Gln
ENST00000699895.1:n.1459C>G
ENST00000699896.1:n.1066+2058C>G
ENST00000699897.1:n.3487C>G
ENST00000392745.8:c.1410C>G MANE Select	ENSP00000376500.3:p.His470Gln
ENST00000347662.8:c.1335C>G	ENSP00000328003.4:p.His445Gln
ENST00000351691.9:c.1335C>G	ENSP00000332468.5:p.His445Gln
ENST00000392745.6:c.1410C>G	ENSP00000376500.2:p.His470Gln
ENST00000539721.5:c.1161C>G	ENSP00000445998.1:p.His387Gln
ENST00000560371.5:c.1410C>G	ENSP00000454207.1:p.His470Gln
NM_001199427.1:c.1161C>G	NP_001186356.1:p.His387Gln
NM_003300.3:c.1410C>G	NP_003291.2:p.His470Gln
NM_145725.2:c.1410C>G , LRG_229t1:c.1410C>G	NP_663777.1:p.His470Gln
NM_145726.2:c.1335C>G	NP_663778.1:p.His445Gln
XM_011537116.1:c.1254C>G	XP_011535418.1:p.His418Gln
XM_011537117.1:c.1242C>G	XP_011535419.1:p.His414Gln
XM_011537118.1:c.1161C>G	XP_011535420.1:p.His387Gln
XM_011537116.3:c.1254C>G	XP_011535418.1:p.His418Gln
XM_011537117.3:c.1242C>G	XP_011535419.1:p.His414Gln
XM_011537118.3:c.1161C>G	XP_011535420.1:p.His387Gln
XM_017021617.1:c.1410C>G	XP_016877106.1:p.His470Gln
XM_017021618.1:c.1410C>G	XP_016877107.1:p.His470Gln
XM_017021619.1:c.1335C>G	XP_016877108.1:p.His445Gln
NM_001199427.2:c.1161C>G	NP_001186356.1:p.His387Gln
NM_003300.4:c.1410C>G	NP_003291.2:p.His470Gln
NM_145725.3:c.1410C>G MANE Select	NP_663777.1:p.His470Gln
NM_001385142.1:c.1269C>G	NP_001372071.1:p.His423Gln
NM_001385143.1:c.1329C>G	NP_001372072.1:p.His443Gln
NM_145726.3:c.1335C>G	NP_663778.1:p.His445Gln