Canonical Allele Identifier: CA351246784
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397657G>C , CM000664.2:g.238397657G>C GRCh38
NC_000002.11:g.239306298G>C , CM000664.1:g.239306298G>C GRCh37
NC_000002.10:g.238971037G>C NCBI36
NG_053055.1:g.82169G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1888G>C MANE Select ENSP00000362424.4:p.Glu630Gln
ENST00000373327.4:c.1888G>C ENSP00000362424.4:p.Glu630Gln
ENST00000391993.7:c.1690G>C ENSP00000375851.3:p.Glu564Gln
ENST00000462122.1:n.899G>C
ENST00000483951.1:n.236G>C
NM_001139490.1:c.1690G>C NP_001132962.1:p.Glu564Gln
NM_015650.3:c.1888G>C NP_056465.2:p.Glu630Gln
XM_006712414.1:c.1687G>C XP_006712477.1:p.Glu563Gln
XM_011510944.1:c.1990G>C XP_011509246.1:p.Glu664Gln
XM_011510945.1:c.1951G>C XP_011509247.1:p.Glu651Gln
XM_011510946.1:c.1918G>C XP_011509248.1:p.Glu640Gln
XM_011510947.1:c.1858G>C XP_011509249.1:p.Glu620Gln
XM_011510948.1:c.1792G>C XP_011509250.1:p.Glu598Gln
XM_011510950.1:c.856G>C XP_011509252.1:p.Glu286Gln
XM_006712414.2:c.1687G>C XP_006712477.1:p.Glu563Gln
XM_011510944.2:c.1990G>C XP_011509246.1:p.Glu664Gln
XM_011510945.2:c.1951G>C XP_011509247.1:p.Glu651Gln
XM_011510946.2:c.1918G>C XP_011509248.1:p.Glu640Gln
XM_011510947.2:c.1858G>C XP_011509249.1:p.Glu620Gln
XM_011510948.2:c.1792G>C XP_011509250.1:p.Glu598Gln
XM_011510950.2:c.856G>C XP_011509252.1:p.Glu286Gln
XM_017003789.1:c.1987G>C XP_016859278.1:p.Glu663Gln
XR_001738696.1:n.1716G>C
XR_001738697.1:n.1713G>C
NM_015650.4:c.1888G>C MANE Select NP_056465.2:p.Glu630Gln