Canonical Allele Identifier: CA2663893652
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397310del , CM000664.2:g.238397310del GRCh38
NC_000002.11:g.239305951del , CM000664.1:g.239305951del GRCh37
NC_000002.10:g.238970690del NCBI36
NG_053055.1:g.81822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1690-149del MANE Select ENSP00000362424.4:n.1690-149del
ENST00000373327.4:c.1690-149del ENSP00000362424.4:n.1690-149del
ENST00000391993.7:c.1492-149del ENSP00000375851.3:n.1492-149del
ENST00000462122.1:n.701-149del
NM_001139490.1:c.1492-149del NP_001132962.1:n.1492-149del
NM_015650.3:c.1690-149del NP_056465.2:n.1690-149del
XM_006712414.1:c.1489-149del XP_006712477.1:n.1489-149del
XM_011510944.1:c.1792-149del XP_011509246.1:n.1792-149del
XM_011510945.1:c.1753-149del XP_011509247.1:n.1753-149del
XM_011510946.1:c.1720-149del XP_011509248.1:n.1720-149del
XM_011510947.1:c.1660-149del XP_011509249.1:n.1660-149del
XM_011510948.1:c.1594-149del XP_011509250.1:n.1594-149del
XM_011510950.1:c.658-149del XP_011509252.1:n.658-149del
XR_922902.1:n.1989-149del
XM_006712414.2:c.1489-149del XP_006712477.1:n.1489-149del
XM_011510944.2:c.1792-149del XP_011509246.1:n.1792-149del
XM_011510945.2:c.1753-149del XP_011509247.1:n.1753-149del
XM_011510946.2:c.1720-149del XP_011509248.1:n.1720-149del
XM_011510947.2:c.1660-149del XP_011509249.1:n.1660-149del
XM_011510948.2:c.1594-149del XP_011509250.1:n.1594-149del
XM_011510950.2:c.658-149del XP_011509252.1:n.658-149del
XM_017003789.1:c.1789-149del XP_016859278.1:n.1789-149del
XR_001738696.1:n.1518-149del
XR_001738697.1:n.1515-149del
XR_922902.2:n.2052-149del
NM_015650.4:c.1690-149del MANE Select NP_056465.2:n.1690-149del