Canonical Allele Identifier: CA351245863

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306143T>C (hg19) ; chr2:g.238397502T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397502T>C , CM000664.2:g.238397502T>C	GRCh38
NC_000002.11:g.239306143T>C , CM000664.1:g.239306143T>C	GRCh37
NC_000002.10:g.238970882T>C	NCBI36
NG_053055.1:g.82014T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1733T>C MANE Select	ENSP00000362424.4:p.Ile578Thr
ENST00000373327.4:c.1733T>C	ENSP00000362424.4:p.Ile578Thr
ENST00000391993.7:c.1535T>C	ENSP00000375851.3:p.Ile512Thr
ENST00000462122.1:n.744T>C
ENST00000483951.1:n.81T>C
NM_001139490.1:c.1535T>C	NP_001132962.1:p.Ile512Thr
NM_015650.3:c.1733T>C	NP_056465.2:p.Ile578Thr
XM_006712414.1:c.1532T>C	XP_006712477.1:p.Ile511Thr
XM_011510944.1:c.1835T>C	XP_011509246.1:p.Ile612Thr
XM_011510945.1:c.1796T>C	XP_011509247.1:p.Ile599Thr
XM_011510946.1:c.1763T>C	XP_011509248.1:p.Ile588Thr
XM_011510947.1:c.1703T>C	XP_011509249.1:p.Ile568Thr
XM_011510948.1:c.1637T>C	XP_011509250.1:p.Ile546Thr
XM_011510950.1:c.701T>C	XP_011509252.1:p.Ile234Thr
XR_922902.1:n.2032T>C
XM_006712414.2:c.1532T>C	XP_006712477.1:p.Ile511Thr
XM_011510944.2:c.1835T>C	XP_011509246.1:p.Ile612Thr
XM_011510945.2:c.1796T>C	XP_011509247.1:p.Ile599Thr
XM_011510946.2:c.1763T>C	XP_011509248.1:p.Ile588Thr
XM_011510947.2:c.1703T>C	XP_011509249.1:p.Ile568Thr
XM_011510948.2:c.1637T>C	XP_011509250.1:p.Ile546Thr
XM_011510950.2:c.701T>C	XP_011509252.1:p.Ile234Thr
XM_017003789.1:c.1832T>C	XP_016859278.1:p.Ile611Thr
XR_001738696.1:n.1561T>C
XR_001738697.1:n.1558T>C
XR_922902.2:n.2095T>C
NM_015650.4:c.1733T>C MANE Select	NP_056465.2:p.Ile578Thr