Canonical Allele Identifier: CA351246682
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397639G>C , CM000664.2:g.238397639G>C GRCh38
NC_000002.11:g.239306280G>C , CM000664.1:g.239306280G>C GRCh37
NC_000002.10:g.238971019G>C NCBI36
NG_053055.1:g.82151G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373327.5:c.1870G>C MANE Select ENSP00000362424.4:p.Glu624Gln
ENST00000373327.4:c.1870G>C ENSP00000362424.4:p.Glu624Gln
ENST00000391993.7:c.1672G>C ENSP00000375851.3:p.Glu558Gln
ENST00000462122.1:n.881G>C
ENST00000483951.1:n.218G>C
NM_001139490.1:c.1672G>C NP_001132962.1:p.Glu558Gln
NM_015650.3:c.1870G>C NP_056465.2:p.Glu624Gln
XM_006712414.1:c.1669G>C XP_006712477.1:p.Glu557Gln
XM_011510944.1:c.1972G>C XP_011509246.1:p.Glu658Gln
XM_011510945.1:c.1933G>C XP_011509247.1:p.Glu645Gln
XM_011510946.1:c.1900G>C XP_011509248.1:p.Glu634Gln
XM_011510947.1:c.1840G>C XP_011509249.1:p.Glu614Gln
XM_011510948.1:c.1774G>C XP_011509250.1:p.Glu592Gln
XM_011510950.1:c.838G>C XP_011509252.1:p.Glu280Gln
XM_006712414.2:c.1669G>C XP_006712477.1:p.Glu557Gln
XM_011510944.2:c.1972G>C XP_011509246.1:p.Glu658Gln
XM_011510945.2:c.1933G>C XP_011509247.1:p.Glu645Gln
XM_011510946.2:c.1900G>C XP_011509248.1:p.Glu634Gln
XM_011510947.2:c.1840G>C XP_011509249.1:p.Glu614Gln
XM_011510948.2:c.1774G>C XP_011509250.1:p.Glu592Gln
XM_011510950.2:c.838G>C XP_011509252.1:p.Glu280Gln
XM_017003789.1:c.1969G>C XP_016859278.1:p.Glu657Gln
XR_001738696.1:n.1698G>C
XR_001738697.1:n.1695G>C
NM_015650.4:c.1870G>C MANE Select NP_056465.2:p.Glu624Gln