Canonical Allele Identifier: CA351245802

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306117G>C (hg19) ; chr2:g.238397476G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397476G>C , CM000664.2:g.238397476G>C	GRCh38
NC_000002.11:g.239306117G>C , CM000664.1:g.239306117G>C	GRCh37
NC_000002.10:g.238970856G>C	NCBI36
NG_053055.1:g.81988G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1707G>C MANE Select	ENSP00000362424.4:p.Glu569Asp
ENST00000373327.4:c.1707G>C	ENSP00000362424.4:p.Glu569Asp
ENST00000391993.7:c.1509G>C	ENSP00000375851.3:p.Glu503Asp
ENST00000462122.1:n.718G>C
ENST00000483951.1:n.55G>C
NM_001139490.1:c.1509G>C	NP_001132962.1:p.Glu503Asp
NM_015650.3:c.1707G>C	NP_056465.2:p.Glu569Asp
XM_006712414.1:c.1506G>C	XP_006712477.1:p.Glu502Asp
XM_011510944.1:c.1809G>C	XP_011509246.1:p.Glu603Asp
XM_011510945.1:c.1770G>C	XP_011509247.1:p.Glu590Asp
XM_011510946.1:c.1737G>C	XP_011509248.1:p.Glu579Asp
XM_011510947.1:c.1677G>C	XP_011509249.1:p.Glu559Asp
XM_011510948.1:c.1611G>C	XP_011509250.1:p.Glu537Asp
XM_011510950.1:c.675G>C	XP_011509252.1:p.Glu225Asp
XR_922902.1:n.2006G>C
XM_006712414.2:c.1506G>C	XP_006712477.1:p.Glu502Asp
XM_011510944.2:c.1809G>C	XP_011509246.1:p.Glu603Asp
XM_011510945.2:c.1770G>C	XP_011509247.1:p.Glu590Asp
XM_011510946.2:c.1737G>C	XP_011509248.1:p.Glu579Asp
XM_011510947.2:c.1677G>C	XP_011509249.1:p.Glu559Asp
XM_011510948.2:c.1611G>C	XP_011509250.1:p.Glu537Asp
XM_011510950.2:c.675G>C	XP_011509252.1:p.Glu225Asp
XM_017003789.1:c.1806G>C	XP_016859278.1:p.Glu602Asp
XR_001738696.1:n.1535G>C
XR_001738697.1:n.1532G>C
XR_922902.2:n.2069G>C
NM_015650.4:c.1707G>C MANE Select	NP_056465.2:p.Glu569Asp