Canonical Allele Identifier: CA351245788

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306112T>A (hg19) ; chr2:g.238397471T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397471T>A , CM000664.2:g.238397471T>A	GRCh38
NC_000002.11:g.239306112T>A , CM000664.1:g.239306112T>A	GRCh37
NC_000002.10:g.238970851T>A	NCBI36
NG_053055.1:g.81983T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1702T>A MANE Select	ENSP00000362424.4:p.Phe568Ile
ENST00000373327.4:c.1702T>A	ENSP00000362424.4:p.Phe568Ile
ENST00000391993.7:c.1504T>A	ENSP00000375851.3:p.Phe502Ile
ENST00000462122.1:n.713T>A
ENST00000483951.1:n.50T>A
NM_001139490.1:c.1504T>A	NP_001132962.1:p.Phe502Ile
NM_015650.3:c.1702T>A	NP_056465.2:p.Phe568Ile
XM_006712414.1:c.1501T>A	XP_006712477.1:p.Phe501Ile
XM_011510944.1:c.1804T>A	XP_011509246.1:p.Phe602Ile
XM_011510945.1:c.1765T>A	XP_011509247.1:p.Phe589Ile
XM_011510946.1:c.1732T>A	XP_011509248.1:p.Phe578Ile
XM_011510947.1:c.1672T>A	XP_011509249.1:p.Phe558Ile
XM_011510948.1:c.1606T>A	XP_011509250.1:p.Phe536Ile
XM_011510950.1:c.670T>A	XP_011509252.1:p.Phe224Ile
XR_922902.1:n.2001T>A
XM_006712414.2:c.1501T>A	XP_006712477.1:p.Phe501Ile
XM_011510944.2:c.1804T>A	XP_011509246.1:p.Phe602Ile
XM_011510945.2:c.1765T>A	XP_011509247.1:p.Phe589Ile
XM_011510946.2:c.1732T>A	XP_011509248.1:p.Phe578Ile
XM_011510947.2:c.1672T>A	XP_011509249.1:p.Phe558Ile
XM_011510948.2:c.1606T>A	XP_011509250.1:p.Phe536Ile
XM_011510950.2:c.670T>A	XP_011509252.1:p.Phe224Ile
XM_017003789.1:c.1801T>A	XP_016859278.1:p.Phe601Ile
XR_001738696.1:n.1530T>A
XR_001738697.1:n.1527T>A
XR_922902.2:n.2064T>A
NM_015650.4:c.1702T>A MANE Select	NP_056465.2:p.Phe568Ile