Canonical Allele Identifier: CA2484358967

Gene: TRAF3IP3

Linked Data

• dbSNP Id: rs2077583620

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209773268A>G , CM000663.2:g.209773268A>G	GRCh38
NC_000001.10:g.209946613A>G , CM000663.1:g.209946613A>G	GRCh37
NC_000001.9:g.208013236A>G	NCBI36
NG_033934.1:g.22237A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367025.8:c.774+249A>G MANE Select	ENSP00000355992.3:n.774+249A>G
ENST00000367023.5:c.-19+249A>G	ENSP00000355990.1:n.-19+249A>G
ENST00000367024.5:c.774+249A>G	ENSP00000355991.1:n.774+249A>G
ENST00000367025.7:c.774+249A>G	ENSP00000355992.3:n.774+249A>G
ENST00000367026.7:c.714+249A>G	ENSP00000355993.3:n.714+249A>G
ENST00000400959.7:c.714+249A>G	ENSP00000383743.3:n.714+249A>G
ENST00000474496.5:n.128+249A>G
ENST00000476050.5:n.138+249A>G
ENST00000477431.1:c.-19+249A>G	ENSP00000417417.1:n.-19+249A>G
ENST00000478359.5:c.774+249A>G	ENSP00000417665.1:n.774+249A>G
ENST00000487271.5:c.-78+249A>G	ENSP00000418906.1:n.-78+249A>G
NM_001287754.1:c.-19+249A>G	NP_001274683.1:n.-19+249A>G
NM_025228.3:c.774+249A>G	NP_079504.2:n.774+249A>G
NR_109871.1:n.1211+249A>G
XM_005273279.3:c.-19+249A>G	XP_005273336.1:n.-19+249A>G
XM_005273280.2:c.-78+249A>G	XP_005273337.1:n.-78+249A>G
XM_011510016.1:c.714+249A>G	XP_011508318.1:n.714+249A>G
XM_011510017.1:c.774+249A>G	XP_011508319.1:n.774+249A>G
XM_011510018.1:c.774+249A>G	XP_011508320.1:n.774+249A>G
XM_011510019.1:c.774+249A>G	XP_011508321.1:n.774+249A>G
XR_247044.1:n.1195+249A>G
NM_001320143.1:c.774+249A>G	NP_001307072.1:n.774+249A>G
NM_001320144.1:c.714+249A>G	NP_001307073.1:n.714+249A>G
XM_005273279.5:c.-19+249A>G	XP_005273336.1:n.-19+249A>G
XM_011510018.3:c.774+249A>G	XP_011508320.1:n.774+249A>G
XM_011510019.2:c.774+249A>G	XP_011508321.1:n.774+249A>G
XM_017002399.2:c.774+249A>G	XP_016857888.1:n.774+249A>G
XM_017002400.2:c.774+249A>G	XP_016857889.1:n.774+249A>G
XM_024449954.1:c.-19+249A>G	XP_024305722.1:n.-19+249A>G
XR_001737438.2:n.1189+249A>G
XR_001737439.2:n.1190+249A>G
XR_001737440.2:n.1190+249A>G
XR_247044.3:n.1190+249A>G
NM_025228.4:c.774+249A>G MANE Select	NP_079504.2:n.774+249A>G
NM_001287754.2:c.-19+249A>G	NP_001274683.1:n.-19+249A>G
NM_001320144.2:c.714+249A>G	NP_001307073.1:n.714+249A>G
NR_109871.2:n.1190+249A>G
NM_001320143.2:c.774+249A>G	NP_001307072.1:n.774+249A>G