Canonical Allele Identifier: CA2577295836

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397373C>A , CM000664.2:g.238397373C>A	GRCh38
NC_000002.11:g.239306014C>A , CM000664.1:g.239306014C>A	GRCh37
NC_000002.10:g.238970753C>A	NCBI36
NG_053055.1:g.81885C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1690-86C>A MANE Select	ENSP00000362424.4:n.1690-86C>A
ENST00000373327.4:c.1690-86C>A	ENSP00000362424.4:n.1690-86C>A
ENST00000391993.7:c.1492-86C>A	ENSP00000375851.3:n.1492-86C>A
ENST00000462122.1:n.701-86C>A
NM_001139490.1:c.1492-86C>A	NP_001132962.1:n.1492-86C>A
NM_015650.3:c.1690-86C>A	NP_056465.2:n.1690-86C>A
XM_006712414.1:c.1489-86C>A	XP_006712477.1:n.1489-86C>A
XM_011510944.1:c.1792-86C>A	XP_011509246.1:n.1792-86C>A
XM_011510945.1:c.1753-86C>A	XP_011509247.1:n.1753-86C>A
XM_011510946.1:c.1720-86C>A	XP_011509248.1:n.1720-86C>A
XM_011510947.1:c.1660-86C>A	XP_011509249.1:n.1660-86C>A
XM_011510948.1:c.1594-86C>A	XP_011509250.1:n.1594-86C>A
XM_011510950.1:c.658-86C>A	XP_011509252.1:n.658-86C>A
XR_922902.1:n.1989-86C>A
XM_006712414.2:c.1489-86C>A	XP_006712477.1:n.1489-86C>A
XM_011510944.2:c.1792-86C>A	XP_011509246.1:n.1792-86C>A
XM_011510945.2:c.1753-86C>A	XP_011509247.1:n.1753-86C>A
XM_011510946.2:c.1720-86C>A	XP_011509248.1:n.1720-86C>A
XM_011510947.2:c.1660-86C>A	XP_011509249.1:n.1660-86C>A
XM_011510948.2:c.1594-86C>A	XP_011509250.1:n.1594-86C>A
XM_011510950.2:c.658-86C>A	XP_011509252.1:n.658-86C>A
XM_017003789.1:c.1789-86C>A	XP_016859278.1:n.1789-86C>A
XR_001738696.1:n.1518-86C>A
XR_001738697.1:n.1515-86C>A
XR_922902.2:n.2052-86C>A
NM_015650.4:c.1690-86C>A MANE Select	NP_056465.2:n.1690-86C>A