Canonical Allele Identifier: CA351245797

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306115G>C (hg19) ; chr2:g.238397474G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397474G>C , CM000664.2:g.238397474G>C	GRCh38
NC_000002.11:g.239306115G>C , CM000664.1:g.239306115G>C	GRCh37
NC_000002.10:g.238970854G>C	NCBI36
NG_053055.1:g.81986G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1705G>C MANE Select	ENSP00000362424.4:p.Glu569Gln
ENST00000373327.4:c.1705G>C	ENSP00000362424.4:p.Glu569Gln
ENST00000391993.7:c.1507G>C	ENSP00000375851.3:p.Glu503Gln
ENST00000462122.1:n.716G>C
ENST00000483951.1:n.53G>C
NM_001139490.1:c.1507G>C	NP_001132962.1:p.Glu503Gln
NM_015650.3:c.1705G>C	NP_056465.2:p.Glu569Gln
XM_006712414.1:c.1504G>C	XP_006712477.1:p.Glu502Gln
XM_011510944.1:c.1807G>C	XP_011509246.1:p.Glu603Gln
XM_011510945.1:c.1768G>C	XP_011509247.1:p.Glu590Gln
XM_011510946.1:c.1735G>C	XP_011509248.1:p.Glu579Gln
XM_011510947.1:c.1675G>C	XP_011509249.1:p.Glu559Gln
XM_011510948.1:c.1609G>C	XP_011509250.1:p.Glu537Gln
XM_011510950.1:c.673G>C	XP_011509252.1:p.Glu225Gln
XR_922902.1:n.2004G>C
XM_006712414.2:c.1504G>C	XP_006712477.1:p.Glu502Gln
XM_011510944.2:c.1807G>C	XP_011509246.1:p.Glu603Gln
XM_011510945.2:c.1768G>C	XP_011509247.1:p.Glu590Gln
XM_011510946.2:c.1735G>C	XP_011509248.1:p.Glu579Gln
XM_011510947.2:c.1675G>C	XP_011509249.1:p.Glu559Gln
XM_011510948.2:c.1609G>C	XP_011509250.1:p.Glu537Gln
XM_011510950.2:c.673G>C	XP_011509252.1:p.Glu225Gln
XM_017003789.1:c.1804G>C	XP_016859278.1:p.Glu602Gln
XR_001738696.1:n.1533G>C
XR_001738697.1:n.1530G>C
XR_922902.2:n.2067G>C
NM_015650.4:c.1705G>C MANE Select	NP_056465.2:p.Glu569Gln