Canonical Allele Identifier: CA351245771

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306102G>C (hg19) ; chr2:g.238397461G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397461G>C , CM000664.2:g.238397461G>C	GRCh38
NC_000002.11:g.239306102G>C , CM000664.1:g.239306102G>C	GRCh37
NC_000002.10:g.238970841G>C	NCBI36
NG_053055.1:g.81973G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1692G>C MANE Select	ENSP00000362424.4:p.Glu564Asp
ENST00000373327.4:c.1692G>C	ENSP00000362424.4:p.Glu564Asp
ENST00000391993.7:c.1494G>C	ENSP00000375851.3:p.Glu498Asp
ENST00000462122.1:n.703G>C
ENST00000483951.1:n.40G>C
NM_001139490.1:c.1494G>C	NP_001132962.1:p.Glu498Asp
NM_015650.3:c.1692G>C	NP_056465.2:p.Glu564Asp
XM_006712414.1:c.1491G>C	XP_006712477.1:p.Glu497Asp
XM_011510944.1:c.1794G>C	XP_011509246.1:p.Glu598Asp
XM_011510945.1:c.1755G>C	XP_011509247.1:p.Glu585Asp
XM_011510946.1:c.1722G>C	XP_011509248.1:p.Glu574Asp
XM_011510947.1:c.1662G>C	XP_011509249.1:p.Glu554Asp
XM_011510948.1:c.1596G>C	XP_011509250.1:p.Glu532Asp
XM_011510950.1:c.660G>C	XP_011509252.1:p.Glu220Asp
XR_922902.1:n.1991G>C
XM_006712414.2:c.1491G>C	XP_006712477.1:p.Glu497Asp
XM_011510944.2:c.1794G>C	XP_011509246.1:p.Glu598Asp
XM_011510945.2:c.1755G>C	XP_011509247.1:p.Glu585Asp
XM_011510946.2:c.1722G>C	XP_011509248.1:p.Glu574Asp
XM_011510947.2:c.1662G>C	XP_011509249.1:p.Glu554Asp
XM_011510948.2:c.1596G>C	XP_011509250.1:p.Glu532Asp
XM_011510950.2:c.660G>C	XP_011509252.1:p.Glu220Asp
XM_017003789.1:c.1791G>C	XP_016859278.1:p.Glu597Asp
XR_001738696.1:n.1520G>C
XR_001738697.1:n.1517G>C
XR_922902.2:n.2054G>C
NM_015650.4:c.1692G>C MANE Select	NP_056465.2:p.Glu564Asp