Canonical Allele Identifier: CA1338105462

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397560A= , CM000664.2:g.238397560A=	GRCh38
NC_000002.11:g.239306201A= , CM000664.1:g.239306201A=	GRCh37
NC_000002.10:g.238970940A=	NCBI36
NG_053055.1:g.82072A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1791A= MANE Select	ENSP00000362424.4:p.Ala597=
ENST00000373327.4:c.1791A=	ENSP00000362424.4:p.Ala597=
ENST00000391993.7:c.1593A=	ENSP00000375851.3:p.Ala531=
ENST00000462122.1:n.802A=
ENST00000483951.1:n.139A=
NM_001139490.1:c.1593A=	NP_001132962.1:p.Ala531=
NM_015650.3:c.1791A=	NP_056465.2:p.Ala597=
XM_006712414.1:c.1590A=	XP_006712477.1:p.Ala530=
XM_011510944.1:c.1893A=	XP_011509246.1:p.Ala631=
XM_011510945.1:c.1854A=	XP_011509247.1:p.Ala618=
XM_011510946.1:c.1821A=	XP_011509248.1:p.Ala607=
XM_011510947.1:c.1761A=	XP_011509249.1:p.Ala587=
XM_011510948.1:c.1695A=	XP_011509250.1:p.Ala565=
XM_011510950.1:c.759A=	XP_011509252.1:p.Ala253=
XM_006712414.2:c.1590A=	XP_006712477.1:p.Ala530=
XM_011510944.2:c.1893A=	XP_011509246.1:p.Ala631=
XM_011510945.2:c.1854A=	XP_011509247.1:p.Ala618=
XM_011510946.2:c.1821A=	XP_011509248.1:p.Ala607=
XM_011510947.2:c.1761A=	XP_011509249.1:p.Ala587=
XM_011510948.2:c.1695A=	XP_011509250.1:p.Ala565=
XM_011510950.2:c.759A=	XP_011509252.1:p.Ala253=
XM_017003789.1:c.1890A=	XP_016859278.1:p.Ala630=
XR_001738696.1:n.1619A=
XR_001738697.1:n.1616A=
NM_015650.4:c.1791A= MANE Select	NP_056465.2:p.Ala597=