Canonical Allele Identifier: CA1338105438

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397517T= , CM000664.2:g.238397517T=	GRCh38
NC_000002.11:g.239306158T= , CM000664.1:g.239306158T=	GRCh37
NC_000002.10:g.238970897T=	NCBI36
NG_053055.1:g.82029T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1748T= MANE Select	ENSP00000362424.4:p.Ile583=
ENST00000373327.4:c.1748T=	ENSP00000362424.4:p.Ile583=
ENST00000391993.7:c.1550T=	ENSP00000375851.3:p.Ile517=
ENST00000462122.1:n.759T=
ENST00000483951.1:n.96T=
NM_001139490.1:c.1550T=	NP_001132962.1:p.Ile517=
NM_015650.3:c.1748T=	NP_056465.2:p.Ile583=
XM_006712414.1:c.1547T=	XP_006712477.1:p.Ile516=
XM_011510944.1:c.1850T=	XP_011509246.1:p.Ile617=
XM_011510945.1:c.1811T=	XP_011509247.1:p.Ile604=
XM_011510946.1:c.1778T=	XP_011509248.1:p.Ile593=
XM_011510947.1:c.1718T=	XP_011509249.1:p.Ile573=
XM_011510948.1:c.1652T=	XP_011509250.1:p.Ile551=
XM_011510950.1:c.716T=	XP_011509252.1:p.Ile239=
XR_922902.1:n.2047T=
XM_006712414.2:c.1547T=	XP_006712477.1:p.Ile516=
XM_011510944.2:c.1850T=	XP_011509246.1:p.Ile617=
XM_011510945.2:c.1811T=	XP_011509247.1:p.Ile604=
XM_011510946.2:c.1778T=	XP_011509248.1:p.Ile593=
XM_011510947.2:c.1718T=	XP_011509249.1:p.Ile573=
XM_011510948.2:c.1652T=	XP_011509250.1:p.Ile551=
XM_011510950.2:c.716T=	XP_011509252.1:p.Ile239=
XM_017003789.1:c.1847T=	XP_016859278.1:p.Ile616=
XR_001738696.1:n.1576T=
XR_001738697.1:n.1573T=
XR_922902.2:n.2110T=
NM_015650.4:c.1748T= MANE Select	NP_056465.2:p.Ile583=