Canonical Allele Identifier: CA351246039

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs144342329
• MyVariant Identifiers: chr2:g.239306180C>G (hg19) ; chr2:g.238397539C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397539C>G , CM000664.2:g.238397539C>G	GRCh38
NC_000002.11:g.239306180C>G , CM000664.1:g.239306180C>G	GRCh37
NC_000002.10:g.238970919C>G	NCBI36
NG_053055.1:g.82051C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1770C>G MANE Select	ENSP00000362424.4:p.Ile590Met
ENST00000373327.4:c.1770C>G	ENSP00000362424.4:p.Ile590Met
ENST00000391993.7:c.1572C>G	ENSP00000375851.3:p.Ile524Met
ENST00000462122.1:n.781C>G
ENST00000483951.1:n.118C>G
NM_001139490.1:c.1572C>G	NP_001132962.1:p.Ile524Met
NM_015650.3:c.1770C>G	NP_056465.2:p.Ile590Met
XM_006712414.1:c.1569C>G	XP_006712477.1:p.Ile523Met
XM_011510944.1:c.1872C>G	XP_011509246.1:p.Ile624Met
XM_011510945.1:c.1833C>G	XP_011509247.1:p.Ile611Met
XM_011510946.1:c.1800C>G	XP_011509248.1:p.Ile600Met
XM_011510947.1:c.1740C>G	XP_011509249.1:p.Ile580Met
XM_011510948.1:c.1674C>G	XP_011509250.1:p.Ile558Met
XM_011510950.1:c.738C>G	XP_011509252.1:p.Ile246Met
XR_922902.1:n.2069C>G
XM_006712414.2:c.1569C>G	XP_006712477.1:p.Ile523Met
XM_011510944.2:c.1872C>G	XP_011509246.1:p.Ile624Met
XM_011510945.2:c.1833C>G	XP_011509247.1:p.Ile611Met
XM_011510946.2:c.1800C>G	XP_011509248.1:p.Ile600Met
XM_011510947.2:c.1740C>G	XP_011509249.1:p.Ile580Met
XM_011510948.2:c.1674C>G	XP_011509250.1:p.Ile558Met
XM_011510950.2:c.738C>G	XP_011509252.1:p.Ile246Met
XM_017003789.1:c.1869C>G	XP_016859278.1:p.Ile623Met
XR_001738696.1:n.1598C>G
XR_001738697.1:n.1595C>G
NM_015650.4:c.1770C>G MANE Select	NP_056465.2:p.Ile590Met