Canonical Allele Identifier: CA1338105431

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397499A= , CM000664.2:g.238397499A=	GRCh38
NC_000002.11:g.239306140A= , CM000664.1:g.239306140A=	GRCh37
NC_000002.10:g.238970879A=	NCBI36
NG_053055.1:g.82011A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1730A= MANE Select	ENSP00000362424.4:p.Asp577=
ENST00000373327.4:c.1730A=	ENSP00000362424.4:p.Asp577=
ENST00000391993.7:c.1532A=	ENSP00000375851.3:p.Asp511=
ENST00000462122.1:n.741A=
ENST00000483951.1:n.78A=
NM_001139490.1:c.1532A=	NP_001132962.1:p.Asp511=
NM_015650.3:c.1730A=	NP_056465.2:p.Asp577=
XM_006712414.1:c.1529A=	XP_006712477.1:p.Asp510=
XM_011510944.1:c.1832A=	XP_011509246.1:p.Asp611=
XM_011510945.1:c.1793A=	XP_011509247.1:p.Asp598=
XM_011510946.1:c.1760A=	XP_011509248.1:p.Asp587=
XM_011510947.1:c.1700A=	XP_011509249.1:p.Asp567=
XM_011510948.1:c.1634A=	XP_011509250.1:p.Asp545=
XM_011510950.1:c.698A=	XP_011509252.1:p.Asp233=
XR_922902.1:n.2029A=
XM_006712414.2:c.1529A=	XP_006712477.1:p.Asp510=
XM_011510944.2:c.1832A=	XP_011509246.1:p.Asp611=
XM_011510945.2:c.1793A=	XP_011509247.1:p.Asp598=
XM_011510946.2:c.1760A=	XP_011509248.1:p.Asp587=
XM_011510947.2:c.1700A=	XP_011509249.1:p.Asp567=
XM_011510948.2:c.1634A=	XP_011509250.1:p.Asp545=
XM_011510950.2:c.698A=	XP_011509252.1:p.Asp233=
XM_017003789.1:c.1829A=	XP_016859278.1:p.Asp610=
XR_001738696.1:n.1558A=
XR_001738697.1:n.1555A=
XR_922902.2:n.2092A=
NM_015650.4:c.1730A= MANE Select	NP_056465.2:p.Asp577=