Canonical Allele Identifier: CA1338105443

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397529G= , CM000664.2:g.238397529G=	GRCh38
NC_000002.11:g.239306170G= , CM000664.1:g.239306170G=	GRCh37
NC_000002.10:g.238970909G=	NCBI36
NG_053055.1:g.82041G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1760G= MANE Select	ENSP00000362424.4:p.Arg587=
ENST00000373327.4:c.1760G=	ENSP00000362424.4:p.Arg587=
ENST00000391993.7:c.1562G=	ENSP00000375851.3:p.Arg521=
ENST00000462122.1:n.771G=
ENST00000483951.1:n.108G=
NM_001139490.1:c.1562G=	NP_001132962.1:p.Arg521=
NM_015650.3:c.1760G=	NP_056465.2:p.Arg587=
XM_006712414.1:c.1559G=	XP_006712477.1:p.Arg520=
XM_011510944.1:c.1862G=	XP_011509246.1:p.Arg621=
XM_011510945.1:c.1823G=	XP_011509247.1:p.Arg608=
XM_011510946.1:c.1790G=	XP_011509248.1:p.Arg597=
XM_011510947.1:c.1730G=	XP_011509249.1:p.Arg577=
XM_011510948.1:c.1664G=	XP_011509250.1:p.Arg555=
XM_011510950.1:c.728G=	XP_011509252.1:p.Arg243=
XR_922902.1:n.2059G=
XM_006712414.2:c.1559G=	XP_006712477.1:p.Arg520=
XM_011510944.2:c.1862G=	XP_011509246.1:p.Arg621=
XM_011510945.2:c.1823G=	XP_011509247.1:p.Arg608=
XM_011510946.2:c.1790G=	XP_011509248.1:p.Arg597=
XM_011510947.2:c.1730G=	XP_011509249.1:p.Arg577=
XM_011510948.2:c.1664G=	XP_011509250.1:p.Arg555=
XM_011510950.2:c.728G=	XP_011509252.1:p.Arg243=
XM_017003789.1:c.1859G=	XP_016859278.1:p.Arg620=
XR_001738696.1:n.1588G=
XR_001738697.1:n.1585G=
NM_015650.4:c.1760G= MANE Select	NP_056465.2:p.Arg587=