Canonical Allele Identifier: CA2663893786
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397700G>C , CM000664.2:g.238397700G>C GRCh38
NC_000002.11:g.239306341G>C , CM000664.1:g.239306341G>C GRCh37
NC_000002.10:g.238971080G>C NCBI36
NG_053055.1:g.82212G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1910+21G>C MANE Select ENSP00000362424.4:n.1910+21G>C
ENST00000373327.4:c.1910+21G>C ENSP00000362424.4:n.1910+21G>C
ENST00000391993.7:c.1712+21G>C ENSP00000375851.3:n.1712+21G>C
ENST00000483951.1:n.258+21G>C
NM_001139490.1:c.1712+21G>C NP_001132962.1:n.1712+21G>C
NM_015650.3:c.1910+21G>C NP_056465.2:n.1910+21G>C
XM_006712414.1:c.1709+21G>C XP_006712477.1:n.1709+21G>C
XM_011510944.1:c.2012+21G>C XP_011509246.1:n.2012+21G>C
XM_011510945.1:c.1973+21G>C XP_011509247.1:n.1973+21G>C
XM_011510946.1:c.1940+21G>C XP_011509248.1:n.1940+21G>C
XM_011510947.1:c.1880+21G>C XP_011509249.1:n.1880+21G>C
XM_011510948.1:c.1814+21G>C XP_011509250.1:n.1814+21G>C
XM_011510950.1:c.878+21G>C XP_011509252.1:n.878+21G>C
XM_006712414.2:c.1709+21G>C XP_006712477.1:n.1709+21G>C
XM_011510944.2:c.2012+21G>C XP_011509246.1:n.2012+21G>C
XM_011510945.2:c.1973+21G>C XP_011509247.1:n.1973+21G>C
XM_011510946.2:c.1940+21G>C XP_011509248.1:n.1940+21G>C
XM_011510947.2:c.1880+21G>C XP_011509249.1:n.1880+21G>C
XM_011510948.2:c.1814+21G>C XP_011509250.1:n.1814+21G>C
XM_011510950.2:c.878+21G>C XP_011509252.1:n.878+21G>C
XM_017003789.1:c.2009+21G>C XP_016859278.1:n.2009+21G>C
XR_001738696.1:n.1738+21G>C
XR_001738697.1:n.1735+21G>C
NM_015650.4:c.1910+21G>C MANE Select NP_056465.2:n.1910+21G>C