Canonical Allele Identifier: CA1338105391

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397427G= , CM000664.2:g.238397427G=	GRCh38
NC_000002.11:g.239306068G= , CM000664.1:g.239306068G=	GRCh37
NC_000002.10:g.238970807G=	NCBI36
NG_053055.1:g.81939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1690-32G= MANE Select	ENSP00000362424.4:n.1690-32G=
ENST00000373327.4:c.1690-32G=	ENSP00000362424.4:n.1690-32G=
ENST00000391993.7:c.1492-32G=	ENSP00000375851.3:n.1492-32G=
ENST00000462122.1:n.701-32G=
ENST00000483951.1:n.6G=
NM_001139490.1:c.1492-32G=	NP_001132962.1:n.1492-32G=
NM_015650.3:c.1690-32G=	NP_056465.2:n.1690-32G=
XM_006712414.1:c.1489-32G=	XP_006712477.1:n.1489-32G=
XM_011510944.1:c.1792-32G=	XP_011509246.1:n.1792-32G=
XM_011510945.1:c.1753-32G=	XP_011509247.1:n.1753-32G=
XM_011510946.1:c.1720-32G=	XP_011509248.1:n.1720-32G=
XM_011510947.1:c.1660-32G=	XP_011509249.1:n.1660-32G=
XM_011510948.1:c.1594-32G=	XP_011509250.1:n.1594-32G=
XM_011510950.1:c.658-32G=	XP_011509252.1:n.658-32G=
XR_922902.1:n.1989-32G=
XM_006712414.2:c.1489-32G=	XP_006712477.1:n.1489-32G=
XM_011510944.2:c.1792-32G=	XP_011509246.1:n.1792-32G=
XM_011510945.2:c.1753-32G=	XP_011509247.1:n.1753-32G=
XM_011510946.2:c.1720-32G=	XP_011509248.1:n.1720-32G=
XM_011510947.2:c.1660-32G=	XP_011509249.1:n.1660-32G=
XM_011510948.2:c.1594-32G=	XP_011509250.1:n.1594-32G=
XM_011510950.2:c.658-32G=	XP_011509252.1:n.658-32G=
XM_017003789.1:c.1789-32G=	XP_016859278.1:n.1789-32G=
XR_001738696.1:n.1518-32G=
XR_001738697.1:n.1515-32G=
XR_922902.2:n.2052-32G=
NM_015650.4:c.1690-32G= MANE Select	NP_056465.2:n.1690-32G=