Canonical Allele Identifier: CA1338105470

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397589T= , CM000664.2:g.238397589T=	GRCh38
NC_000002.11:g.239306230T= , CM000664.1:g.239306230T=	GRCh37
NC_000002.10:g.238970969T=	NCBI36
NG_053055.1:g.82101T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1820T= MANE Select	ENSP00000362424.4:p.Ile607=
ENST00000373327.4:c.1820T=	ENSP00000362424.4:p.Ile607=
ENST00000391993.7:c.1622T=	ENSP00000375851.3:p.Ile541=
ENST00000462122.1:n.831T=
ENST00000483951.1:n.168T=
NM_001139490.1:c.1622T=	NP_001132962.1:p.Ile541=
NM_015650.3:c.1820T=	NP_056465.2:p.Ile607=
XM_006712414.1:c.1619T=	XP_006712477.1:p.Ile540=
XM_011510944.1:c.1922T=	XP_011509246.1:p.Ile641=
XM_011510945.1:c.1883T=	XP_011509247.1:p.Ile628=
XM_011510946.1:c.1850T=	XP_011509248.1:p.Ile617=
XM_011510947.1:c.1790T=	XP_011509249.1:p.Ile597=
XM_011510948.1:c.1724T=	XP_011509250.1:p.Ile575=
XM_011510950.1:c.788T=	XP_011509252.1:p.Ile263=
XM_006712414.2:c.1619T=	XP_006712477.1:p.Ile540=
XM_011510944.2:c.1922T=	XP_011509246.1:p.Ile641=
XM_011510945.2:c.1883T=	XP_011509247.1:p.Ile628=
XM_011510946.2:c.1850T=	XP_011509248.1:p.Ile617=
XM_011510947.2:c.1790T=	XP_011509249.1:p.Ile597=
XM_011510948.2:c.1724T=	XP_011509250.1:p.Ile575=
XM_011510950.2:c.788T=	XP_011509252.1:p.Ile263=
XM_017003789.1:c.1919T=	XP_016859278.1:p.Ile640=
XR_001738696.1:n.1648T=
XR_001738697.1:n.1645T=
NM_015650.4:c.1820T= MANE Select	NP_056465.2:p.Ile607=