Canonical Allele Identifier: CA2663893715
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397353C>G , CM000664.2:g.238397353C>G GRCh38
NC_000002.11:g.239305994C>G , CM000664.1:g.239305994C>G GRCh37
NC_000002.10:g.238970733C>G NCBI36
NG_053055.1:g.81865C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1690-106C>G MANE Select ENSP00000362424.4:n.1690-106C>G
ENST00000373327.4:c.1690-106C>G ENSP00000362424.4:n.1690-106C>G
ENST00000391993.7:c.1492-106C>G ENSP00000375851.3:n.1492-106C>G
ENST00000462122.1:n.701-106C>G
NM_001139490.1:c.1492-106C>G NP_001132962.1:n.1492-106C>G
NM_015650.3:c.1690-106C>G NP_056465.2:n.1690-106C>G
XM_006712414.1:c.1489-106C>G XP_006712477.1:n.1489-106C>G
XM_011510944.1:c.1792-106C>G XP_011509246.1:n.1792-106C>G
XM_011510945.1:c.1753-106C>G XP_011509247.1:n.1753-106C>G
XM_011510946.1:c.1720-106C>G XP_011509248.1:n.1720-106C>G
XM_011510947.1:c.1660-106C>G XP_011509249.1:n.1660-106C>G
XM_011510948.1:c.1594-106C>G XP_011509250.1:n.1594-106C>G
XM_011510950.1:c.658-106C>G XP_011509252.1:n.658-106C>G
XR_922902.1:n.1989-106C>G
XM_006712414.2:c.1489-106C>G XP_006712477.1:n.1489-106C>G
XM_011510944.2:c.1792-106C>G XP_011509246.1:n.1792-106C>G
XM_011510945.2:c.1753-106C>G XP_011509247.1:n.1753-106C>G
XM_011510946.2:c.1720-106C>G XP_011509248.1:n.1720-106C>G
XM_011510947.2:c.1660-106C>G XP_011509249.1:n.1660-106C>G
XM_011510948.2:c.1594-106C>G XP_011509250.1:n.1594-106C>G
XM_011510950.2:c.658-106C>G XP_011509252.1:n.658-106C>G
XM_017003789.1:c.1789-106C>G XP_016859278.1:n.1789-106C>G
XR_001738696.1:n.1518-106C>G
XR_001738697.1:n.1515-106C>G
XR_922902.2:n.2052-106C>G
NM_015650.4:c.1690-106C>G MANE Select NP_056465.2:n.1690-106C>G