Canonical Allele Identifier: CA1338105411

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397463G= , CM000664.2:g.238397463G=	GRCh38
NC_000002.11:g.239306104G= , CM000664.1:g.239306104G=	GRCh37
NC_000002.10:g.238970843G=	NCBI36
NG_053055.1:g.81975G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1694G= MANE Select	ENSP00000362424.4:p.Arg565=
ENST00000373327.4:c.1694G=	ENSP00000362424.4:p.Arg565=
ENST00000391993.7:c.1496G=	ENSP00000375851.3:p.Arg499=
ENST00000462122.1:n.705G=
ENST00000483951.1:n.42G=
NM_001139490.1:c.1496G=	NP_001132962.1:p.Arg499=
NM_015650.3:c.1694G=	NP_056465.2:p.Arg565=
XM_006712414.1:c.1493G=	XP_006712477.1:p.Arg498=
XM_011510944.1:c.1796G=	XP_011509246.1:p.Arg599=
XM_011510945.1:c.1757G=	XP_011509247.1:p.Arg586=
XM_011510946.1:c.1724G=	XP_011509248.1:p.Arg575=
XM_011510947.1:c.1664G=	XP_011509249.1:p.Arg555=
XM_011510948.1:c.1598G=	XP_011509250.1:p.Arg533=
XM_011510950.1:c.662G=	XP_011509252.1:p.Arg221=
XR_922902.1:n.1993G=
XM_006712414.2:c.1493G=	XP_006712477.1:p.Arg498=
XM_011510944.2:c.1796G=	XP_011509246.1:p.Arg599=
XM_011510945.2:c.1757G=	XP_011509247.1:p.Arg586=
XM_011510946.2:c.1724G=	XP_011509248.1:p.Arg575=
XM_011510947.2:c.1664G=	XP_011509249.1:p.Arg555=
XM_011510948.2:c.1598G=	XP_011509250.1:p.Arg533=
XM_011510950.2:c.662G=	XP_011509252.1:p.Arg221=
XM_017003789.1:c.1793G=	XP_016859278.1:p.Arg598=
XR_001738696.1:n.1522G=
XR_001738697.1:n.1519G=
XR_922902.2:n.2056G=
NM_015650.4:c.1694G= MANE Select	NP_056465.2:p.Arg565=