Canonical Allele Identifier: CA1338105306
Gene: TRAF3IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397308C= , CM000664.2:g.238397308C= GRCh38
NC_000002.11:g.239305949C= , CM000664.1:g.239305949C= GRCh37
NC_000002.10:g.238970688C= NCBI36
NG_053055.1:g.81820C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1690-151C= MANE Select ENSP00000362424.4:n.1690-151C=
ENST00000373327.4:c.1690-151C= ENSP00000362424.4:n.1690-151C=
ENST00000391993.7:c.1492-151C= ENSP00000375851.3:n.1492-151C=
ENST00000462122.1:n.701-151C=
NM_001139490.1:c.1492-151C= NP_001132962.1:n.1492-151C=
NM_015650.3:c.1690-151C= NP_056465.2:n.1690-151C=
XM_006712414.1:c.1489-151C= XP_006712477.1:n.1489-151C=
XM_011510944.1:c.1792-151C= XP_011509246.1:n.1792-151C=
XM_011510945.1:c.1753-151C= XP_011509247.1:n.1753-151C=
XM_011510946.1:c.1720-151C= XP_011509248.1:n.1720-151C=
XM_011510947.1:c.1660-151C= XP_011509249.1:n.1660-151C=
XM_011510948.1:c.1594-151C= XP_011509250.1:n.1594-151C=
XM_011510950.1:c.658-151C= XP_011509252.1:n.658-151C=
XR_922902.1:n.1989-151C=
XM_006712414.2:c.1489-151C= XP_006712477.1:n.1489-151C=
XM_011510944.2:c.1792-151C= XP_011509246.1:n.1792-151C=
XM_011510945.2:c.1753-151C= XP_011509247.1:n.1753-151C=
XM_011510946.2:c.1720-151C= XP_011509248.1:n.1720-151C=
XM_011510947.2:c.1660-151C= XP_011509249.1:n.1660-151C=
XM_011510948.2:c.1594-151C= XP_011509250.1:n.1594-151C=
XM_011510950.2:c.658-151C= XP_011509252.1:n.658-151C=
XM_017003789.1:c.1789-151C= XP_016859278.1:n.1789-151C=
XR_001738696.1:n.1518-151C=
XR_001738697.1:n.1515-151C=
XR_922902.2:n.2052-151C=
NM_015650.4:c.1690-151C= MANE Select NP_056465.2:n.1690-151C=