Canonical Allele Identifier: CA351246070
Gene: TRAF3IP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397546C>A , CM000664.2:g.238397546C>A GRCh38
NC_000002.11:g.239306187C>A , CM000664.1:g.239306187C>A GRCh37
NC_000002.10:g.238970926C>A NCBI36
NG_053055.1:g.82058C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1777C>A MANE Select ENSP00000362424.4:p.Leu593Met
ENST00000373327.4:c.1777C>A ENSP00000362424.4:p.Leu593Met
ENST00000391993.7:c.1579C>A ENSP00000375851.3:p.Leu527Met
ENST00000462122.1:n.788C>A
ENST00000483951.1:n.125C>A
NM_001139490.1:c.1579C>A NP_001132962.1:p.Leu527Met
NM_015650.3:c.1777C>A NP_056465.2:p.Leu593Met
XM_006712414.1:c.1576C>A XP_006712477.1:p.Leu526Met
XM_011510944.1:c.1879C>A XP_011509246.1:p.Leu627Met
XM_011510945.1:c.1840C>A XP_011509247.1:p.Leu614Met
XM_011510946.1:c.1807C>A XP_011509248.1:p.Leu603Met
XM_011510947.1:c.1747C>A XP_011509249.1:p.Leu583Met
XM_011510948.1:c.1681C>A XP_011509250.1:p.Leu561Met
XM_011510950.1:c.745C>A XP_011509252.1:p.Leu249Met
XM_006712414.2:c.1576C>A XP_006712477.1:p.Leu526Met
XM_011510944.2:c.1879C>A XP_011509246.1:p.Leu627Met
XM_011510945.2:c.1840C>A XP_011509247.1:p.Leu614Met
XM_011510946.2:c.1807C>A XP_011509248.1:p.Leu603Met
XM_011510947.2:c.1747C>A XP_011509249.1:p.Leu583Met
XM_011510948.2:c.1681C>A XP_011509250.1:p.Leu561Met
XM_011510950.2:c.745C>A XP_011509252.1:p.Leu249Met
XM_017003789.1:c.1876C>A XP_016859278.1:p.Leu626Met
XR_001738696.1:n.1605C>A
XR_001738697.1:n.1602C>A
NM_015650.4:c.1777C>A MANE Select NP_056465.2:p.Leu593Met