Canonical Allele Identifier: CA351246030

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306179T>C (hg19) ; chr2:g.238397538T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397538T>C , CM000664.2:g.238397538T>C	GRCh38
NC_000002.11:g.239306179T>C , CM000664.1:g.239306179T>C	GRCh37
NC_000002.10:g.238970918T>C	NCBI36
NG_053055.1:g.82050T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1769T>C MANE Select	ENSP00000362424.4:p.Ile590Thr
ENST00000373327.4:c.1769T>C	ENSP00000362424.4:p.Ile590Thr
ENST00000391993.7:c.1571T>C	ENSP00000375851.3:p.Ile524Thr
ENST00000462122.1:n.780T>C
ENST00000483951.1:n.117T>C
NM_001139490.1:c.1571T>C	NP_001132962.1:p.Ile524Thr
NM_015650.3:c.1769T>C	NP_056465.2:p.Ile590Thr
XM_006712414.1:c.1568T>C	XP_006712477.1:p.Ile523Thr
XM_011510944.1:c.1871T>C	XP_011509246.1:p.Ile624Thr
XM_011510945.1:c.1832T>C	XP_011509247.1:p.Ile611Thr
XM_011510946.1:c.1799T>C	XP_011509248.1:p.Ile600Thr
XM_011510947.1:c.1739T>C	XP_011509249.1:p.Ile580Thr
XM_011510948.1:c.1673T>C	XP_011509250.1:p.Ile558Thr
XM_011510950.1:c.737T>C	XP_011509252.1:p.Ile246Thr
XR_922902.1:n.2068T>C
XM_006712414.2:c.1568T>C	XP_006712477.1:p.Ile523Thr
XM_011510944.2:c.1871T>C	XP_011509246.1:p.Ile624Thr
XM_011510945.2:c.1832T>C	XP_011509247.1:p.Ile611Thr
XM_011510946.2:c.1799T>C	XP_011509248.1:p.Ile600Thr
XM_011510947.2:c.1739T>C	XP_011509249.1:p.Ile580Thr
XM_011510948.2:c.1673T>C	XP_011509250.1:p.Ile558Thr
XM_011510950.2:c.737T>C	XP_011509252.1:p.Ile246Thr
XM_017003789.1:c.1868T>C	XP_016859278.1:p.Ile623Thr
XR_001738696.1:n.1597T>C
XR_001738697.1:n.1594T>C
NM_015650.4:c.1769T>C MANE Select	NP_056465.2:p.Ile590Thr