Canonical Allele Identifier: CA1338105328
Gene: TRAF3IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397349C= , CM000664.2:g.238397349C= GRCh38
NC_000002.11:g.239305990C= , CM000664.1:g.239305990C= GRCh37
NC_000002.10:g.238970729C= NCBI36
NG_053055.1:g.81861C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1690-110C= MANE Select ENSP00000362424.4:n.1690-110C=
ENST00000373327.4:c.1690-110C= ENSP00000362424.4:n.1690-110C=
ENST00000391993.7:c.1492-110C= ENSP00000375851.3:n.1492-110C=
ENST00000462122.1:n.701-110C=
NM_001139490.1:c.1492-110C= NP_001132962.1:n.1492-110C=
NM_015650.3:c.1690-110C= NP_056465.2:n.1690-110C=
XM_006712414.1:c.1489-110C= XP_006712477.1:n.1489-110C=
XM_011510944.1:c.1792-110C= XP_011509246.1:n.1792-110C=
XM_011510945.1:c.1753-110C= XP_011509247.1:n.1753-110C=
XM_011510946.1:c.1720-110C= XP_011509248.1:n.1720-110C=
XM_011510947.1:c.1660-110C= XP_011509249.1:n.1660-110C=
XM_011510948.1:c.1594-110C= XP_011509250.1:n.1594-110C=
XM_011510950.1:c.658-110C= XP_011509252.1:n.658-110C=
XR_922902.1:n.1989-110C=
XM_006712414.2:c.1489-110C= XP_006712477.1:n.1489-110C=
XM_011510944.2:c.1792-110C= XP_011509246.1:n.1792-110C=
XM_011510945.2:c.1753-110C= XP_011509247.1:n.1753-110C=
XM_011510946.2:c.1720-110C= XP_011509248.1:n.1720-110C=
XM_011510947.2:c.1660-110C= XP_011509249.1:n.1660-110C=
XM_011510948.2:c.1594-110C= XP_011509250.1:n.1594-110C=
XM_011510950.2:c.658-110C= XP_011509252.1:n.658-110C=
XM_017003789.1:c.1789-110C= XP_016859278.1:n.1789-110C=
XR_001738696.1:n.1518-110C=
XR_001738697.1:n.1515-110C=
XR_922902.2:n.2052-110C=
NM_015650.4:c.1690-110C= MANE Select NP_056465.2:n.1690-110C=