Canonical Allele Identifier: CA2663893670
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397320G>T , CM000664.2:g.238397320G>T GRCh38
NC_000002.11:g.239305961G>T , CM000664.1:g.239305961G>T GRCh37
NC_000002.10:g.238970700G>T NCBI36
NG_053055.1:g.81832G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1690-139G>T MANE Select ENSP00000362424.4:n.1690-139G>T
ENST00000373327.4:c.1690-139G>T ENSP00000362424.4:n.1690-139G>T
ENST00000391993.7:c.1492-139G>T ENSP00000375851.3:n.1492-139G>T
ENST00000462122.1:n.701-139G>T
NM_001139490.1:c.1492-139G>T NP_001132962.1:n.1492-139G>T
NM_015650.3:c.1690-139G>T NP_056465.2:n.1690-139G>T
XM_006712414.1:c.1489-139G>T XP_006712477.1:n.1489-139G>T
XM_011510944.1:c.1792-139G>T XP_011509246.1:n.1792-139G>T
XM_011510945.1:c.1753-139G>T XP_011509247.1:n.1753-139G>T
XM_011510946.1:c.1720-139G>T XP_011509248.1:n.1720-139G>T
XM_011510947.1:c.1660-139G>T XP_011509249.1:n.1660-139G>T
XM_011510948.1:c.1594-139G>T XP_011509250.1:n.1594-139G>T
XM_011510950.1:c.658-139G>T XP_011509252.1:n.658-139G>T
XR_922902.1:n.1989-139G>T
XM_006712414.2:c.1489-139G>T XP_006712477.1:n.1489-139G>T
XM_011510944.2:c.1792-139G>T XP_011509246.1:n.1792-139G>T
XM_011510945.2:c.1753-139G>T XP_011509247.1:n.1753-139G>T
XM_011510946.2:c.1720-139G>T XP_011509248.1:n.1720-139G>T
XM_011510947.2:c.1660-139G>T XP_011509249.1:n.1660-139G>T
XM_011510948.2:c.1594-139G>T XP_011509250.1:n.1594-139G>T
XM_011510950.2:c.658-139G>T XP_011509252.1:n.658-139G>T
XM_017003789.1:c.1789-139G>T XP_016859278.1:n.1789-139G>T
XR_001738696.1:n.1518-139G>T
XR_001738697.1:n.1515-139G>T
XR_922902.2:n.2052-139G>T
NM_015650.4:c.1690-139G>T MANE Select NP_056465.2:n.1690-139G>T