Canonical Allele Identifier: CA351245867

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306145G>T (hg19) ; chr2:g.238397504G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397504G>T , CM000664.2:g.238397504G>T	GRCh38
NC_000002.11:g.239306145G>T , CM000664.1:g.239306145G>T	GRCh37
NC_000002.10:g.238970884G>T	NCBI36
NG_053055.1:g.82016G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1735G>T MANE Select	ENSP00000362424.4:p.Val579Phe
ENST00000373327.4:c.1735G>T	ENSP00000362424.4:p.Val579Phe
ENST00000391993.7:c.1537G>T	ENSP00000375851.3:p.Val513Phe
ENST00000462122.1:n.746G>T
ENST00000483951.1:n.83G>T
NM_001139490.1:c.1537G>T	NP_001132962.1:p.Val513Phe
NM_015650.3:c.1735G>T	NP_056465.2:p.Val579Phe
XM_006712414.1:c.1534G>T	XP_006712477.1:p.Val512Phe
XM_011510944.1:c.1837G>T	XP_011509246.1:p.Val613Phe
XM_011510945.1:c.1798G>T	XP_011509247.1:p.Val600Phe
XM_011510946.1:c.1765G>T	XP_011509248.1:p.Val589Phe
XM_011510947.1:c.1705G>T	XP_011509249.1:p.Val569Phe
XM_011510948.1:c.1639G>T	XP_011509250.1:p.Val547Phe
XM_011510950.1:c.703G>T	XP_011509252.1:p.Val235Phe
XR_922902.1:n.2034G>T
XM_006712414.2:c.1534G>T	XP_006712477.1:p.Val512Phe
XM_011510944.2:c.1837G>T	XP_011509246.1:p.Val613Phe
XM_011510945.2:c.1798G>T	XP_011509247.1:p.Val600Phe
XM_011510946.2:c.1765G>T	XP_011509248.1:p.Val589Phe
XM_011510947.2:c.1705G>T	XP_011509249.1:p.Val569Phe
XM_011510948.2:c.1639G>T	XP_011509250.1:p.Val547Phe
XM_011510950.2:c.703G>T	XP_011509252.1:p.Val235Phe
XM_017003789.1:c.1834G>T	XP_016859278.1:p.Val612Phe
XR_001738696.1:n.1563G>T
XR_001738697.1:n.1560G>T
XR_922902.2:n.2097G>T
NM_015650.4:c.1735G>T MANE Select	NP_056465.2:p.Val579Phe