Canonical Allele Identifier: CA351246877

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306320G>C (hg19) ; chr2:g.238397679G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397679G>C , CM000664.2:g.238397679G>C	GRCh38
NC_000002.11:g.239306320G>C , CM000664.1:g.239306320G>C	GRCh37
NC_000002.10:g.238971059G>C	NCBI36
NG_053055.1:g.82191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1910G>C MANE Select	ENSP00000362424.4:p.Arg637Thr
ENST00000373327.4:c.1910G>C	ENSP00000362424.4:p.Arg637Thr
ENST00000391993.7:c.1712G>C	ENSP00000375851.3:p.Arg571Thr
ENST00000462122.1:n.921G>C
ENST00000483951.1:n.258G>C
NM_001139490.1:c.1712G>C	NP_001132962.1:p.Arg571Thr
NM_015650.3:c.1910G>C	NP_056465.2:p.Arg637Thr
XM_006712414.1:c.1709G>C	XP_006712477.1:p.Arg570Thr
XM_011510944.1:c.2012G>C	XP_011509246.1:p.Arg671Thr
XM_011510945.1:c.1973G>C	XP_011509247.1:p.Arg658Thr
XM_011510946.1:c.1940G>C	XP_011509248.1:p.Arg647Thr
XM_011510947.1:c.1880G>C	XP_011509249.1:p.Arg627Thr
XM_011510948.1:c.1814G>C	XP_011509250.1:p.Arg605Thr
XM_011510950.1:c.878G>C	XP_011509252.1:p.Arg293Thr
XM_006712414.2:c.1709G>C	XP_006712477.1:p.Arg570Thr
XM_011510944.2:c.2012G>C	XP_011509246.1:p.Arg671Thr
XM_011510945.2:c.1973G>C	XP_011509247.1:p.Arg658Thr
XM_011510946.2:c.1940G>C	XP_011509248.1:p.Arg647Thr
XM_011510947.2:c.1880G>C	XP_011509249.1:p.Arg627Thr
XM_011510948.2:c.1814G>C	XP_011509250.1:p.Arg605Thr
XM_011510950.2:c.878G>C	XP_011509252.1:p.Arg293Thr
XM_017003789.1:c.2009G>C	XP_016859278.1:p.Arg670Thr
XR_001738696.1:n.1738G>C
XR_001738697.1:n.1735G>C
NM_015650.4:c.1910G>C MANE Select	NP_056465.2:p.Arg637Thr