Canonical Allele Identifier: CA2740096505
Gene: TRAF3IP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3010811
ClinVar RCV Id: RCV003862450

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397627_238397629delinsCTA , CM000664.2:g.238397627_238397629delinsCTA GRCh38
NC_000002.11:g.239306268_239306270delinsCTA , CM000664.1:g.239306268_239306270delinsCTA GRCh37
NC_000002.10:g.238971007_238971009delinsCTA NCBI36
NG_053055.1:g.82139_82141delinsCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000373327.5:c.1858_1860delinsCTA MANE Select ENSP00000362424.4:p.Met620Leu
ENST00000373327.4:c.1858_1860delinsCTA ENSP00000362424.4:p.Met620Leu
ENST00000391993.7:c.1660_1662delinsCTA ENSP00000375851.3:p.Met554Leu
ENST00000462122.1:n.869_871delinsCTA
ENST00000483951.1:n.206_208delinsCTA
NM_001139490.1:c.1660_1662delinsCTA NP_001132962.1:p.Met554Leu
NM_015650.3:c.1858_1860delinsCTA NP_056465.2:p.Met620Leu
XM_006712414.1:c.1657_1659delinsCTA XP_006712477.1:p.Met553Leu
XM_011510944.1:c.1960_1962delinsCTA XP_011509246.1:p.Met654Leu
XM_011510945.1:c.1921_1923delinsCTA XP_011509247.1:p.Met641Leu
XM_011510946.1:c.1888_1890delinsCTA XP_011509248.1:p.Met630Leu
XM_011510947.1:c.1828_1830delinsCTA XP_011509249.1:p.Met610Leu
XM_011510948.1:c.1762_1764delinsCTA XP_011509250.1:p.Met588Leu
XM_011510950.1:c.826_828delinsCTA XP_011509252.1:p.Met276Leu
XM_006712414.2:c.1657_1659delinsCTA XP_006712477.1:p.Met553Leu
XM_011510944.2:c.1960_1962delinsCTA XP_011509246.1:p.Met654Leu
XM_011510945.2:c.1921_1923delinsCTA XP_011509247.1:p.Met641Leu
XM_011510946.2:c.1888_1890delinsCTA XP_011509248.1:p.Met630Leu
XM_011510947.2:c.1828_1830delinsCTA XP_011509249.1:p.Met610Leu
XM_011510948.2:c.1762_1764delinsCTA XP_011509250.1:p.Met588Leu
XM_011510950.2:c.826_828delinsCTA XP_011509252.1:p.Met276Leu
XM_017003789.1:c.1957_1959delinsCTA XP_016859278.1:p.Met653Leu
XR_001738696.1:n.1686_1688delinsCTA
XR_001738697.1:n.1683_1685delinsCTA
NM_015650.4:c.1858_1860delinsCTA MANE Select NP_056465.2:p.Met620Leu