Canonical Allele Identifier: CA351245860

Gene: TRAF3IP1

Linked Data

• gnomAD v4: 2-238397501-A-G
• MyVariant Identifiers: chr2:g.239306142A>G (hg19) ; chr2:g.238397501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397501A>G , CM000664.2:g.238397501A>G	GRCh38
NC_000002.11:g.239306142A>G , CM000664.1:g.239306142A>G	GRCh37
NC_000002.10:g.238970881A>G	NCBI36
NG_053055.1:g.82013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1732A>G MANE Select	ENSP00000362424.4:p.Ile578Val
ENST00000373327.4:c.1732A>G	ENSP00000362424.4:p.Ile578Val
ENST00000391993.7:c.1534A>G	ENSP00000375851.3:p.Ile512Val
ENST00000462122.1:n.743A>G
ENST00000483951.1:n.80A>G
NM_001139490.1:c.1534A>G	NP_001132962.1:p.Ile512Val
NM_015650.3:c.1732A>G	NP_056465.2:p.Ile578Val
XM_006712414.1:c.1531A>G	XP_006712477.1:p.Ile511Val
XM_011510944.1:c.1834A>G	XP_011509246.1:p.Ile612Val
XM_011510945.1:c.1795A>G	XP_011509247.1:p.Ile599Val
XM_011510946.1:c.1762A>G	XP_011509248.1:p.Ile588Val
XM_011510947.1:c.1702A>G	XP_011509249.1:p.Ile568Val
XM_011510948.1:c.1636A>G	XP_011509250.1:p.Ile546Val
XM_011510950.1:c.700A>G	XP_011509252.1:p.Ile234Val
XR_922902.1:n.2031A>G
XM_006712414.2:c.1531A>G	XP_006712477.1:p.Ile511Val
XM_011510944.2:c.1834A>G	XP_011509246.1:p.Ile612Val
XM_011510945.2:c.1795A>G	XP_011509247.1:p.Ile599Val
XM_011510946.2:c.1762A>G	XP_011509248.1:p.Ile588Val
XM_011510947.2:c.1702A>G	XP_011509249.1:p.Ile568Val
XM_011510948.2:c.1636A>G	XP_011509250.1:p.Ile546Val
XM_011510950.2:c.700A>G	XP_011509252.1:p.Ile234Val
XM_017003789.1:c.1831A>G	XP_016859278.1:p.Ile611Val
XR_001738696.1:n.1560A>G
XR_001738697.1:n.1557A>G
XR_922902.2:n.2094A>G
NM_015650.4:c.1732A>G MANE Select	NP_056465.2:p.Ile578Val