Canonical Allele Identifier: CA2577295855

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397438C>G , CM000664.2:g.238397438C>G	GRCh38
NC_000002.11:g.239306079C>G , CM000664.1:g.239306079C>G	GRCh37
NC_000002.10:g.238970818C>G	NCBI36
NG_053055.1:g.81950C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1690-21C>G MANE Select	ENSP00000362424.4:n.1690-21C>G
ENST00000373327.4:c.1690-21C>G	ENSP00000362424.4:n.1690-21C>G
ENST00000391993.7:c.1492-21C>G	ENSP00000375851.3:n.1492-21C>G
ENST00000462122.1:n.701-21C>G
ENST00000483951.1:n.17C>G
NM_001139490.1:c.1492-21C>G	NP_001132962.1:n.1492-21C>G
NM_015650.3:c.1690-21C>G	NP_056465.2:n.1690-21C>G
XM_006712414.1:c.1489-21C>G	XP_006712477.1:n.1489-21C>G
XM_011510944.1:c.1792-21C>G	XP_011509246.1:n.1792-21C>G
XM_011510945.1:c.1753-21C>G	XP_011509247.1:n.1753-21C>G
XM_011510946.1:c.1720-21C>G	XP_011509248.1:n.1720-21C>G
XM_011510947.1:c.1660-21C>G	XP_011509249.1:n.1660-21C>G
XM_011510948.1:c.1594-21C>G	XP_011509250.1:n.1594-21C>G
XM_011510950.1:c.658-21C>G	XP_011509252.1:n.658-21C>G
XR_922902.1:n.1989-21C>G
XM_006712414.2:c.1489-21C>G	XP_006712477.1:n.1489-21C>G
XM_011510944.2:c.1792-21C>G	XP_011509246.1:n.1792-21C>G
XM_011510945.2:c.1753-21C>G	XP_011509247.1:n.1753-21C>G
XM_011510946.2:c.1720-21C>G	XP_011509248.1:n.1720-21C>G
XM_011510947.2:c.1660-21C>G	XP_011509249.1:n.1660-21C>G
XM_011510948.2:c.1594-21C>G	XP_011509250.1:n.1594-21C>G
XM_011510950.2:c.658-21C>G	XP_011509252.1:n.658-21C>G
XM_017003789.1:c.1789-21C>G	XP_016859278.1:n.1789-21C>G
XR_001738696.1:n.1518-21C>G
XR_001738697.1:n.1515-21C>G
XR_922902.2:n.2052-21C>G
NM_015650.4:c.1690-21C>G MANE Select	NP_056465.2:n.1690-21C>G