Canonical Allele Identifier: CA351246339

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs1701287059
• MyVariant Identifiers: chr2:g.239306230T>C (hg19) ; chr2:g.238397589T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397589T>C , CM000664.2:g.238397589T>C	GRCh38
NC_000002.11:g.239306230T>C , CM000664.1:g.239306230T>C	GRCh37
NC_000002.10:g.238970969T>C	NCBI36
NG_053055.1:g.82101T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1820T>C MANE Select	ENSP00000362424.4:p.Ile607Thr
ENST00000373327.4:c.1820T>C	ENSP00000362424.4:p.Ile607Thr
ENST00000391993.7:c.1622T>C	ENSP00000375851.3:p.Ile541Thr
ENST00000462122.1:n.831T>C
ENST00000483951.1:n.168T>C
NM_001139490.1:c.1622T>C	NP_001132962.1:p.Ile541Thr
NM_015650.3:c.1820T>C	NP_056465.2:p.Ile607Thr
XM_006712414.1:c.1619T>C	XP_006712477.1:p.Ile540Thr
XM_011510944.1:c.1922T>C	XP_011509246.1:p.Ile641Thr
XM_011510945.1:c.1883T>C	XP_011509247.1:p.Ile628Thr
XM_011510946.1:c.1850T>C	XP_011509248.1:p.Ile617Thr
XM_011510947.1:c.1790T>C	XP_011509249.1:p.Ile597Thr
XM_011510948.1:c.1724T>C	XP_011509250.1:p.Ile575Thr
XM_011510950.1:c.788T>C	XP_011509252.1:p.Ile263Thr
XM_006712414.2:c.1619T>C	XP_006712477.1:p.Ile540Thr
XM_011510944.2:c.1922T>C	XP_011509246.1:p.Ile641Thr
XM_011510945.2:c.1883T>C	XP_011509247.1:p.Ile628Thr
XM_011510946.2:c.1850T>C	XP_011509248.1:p.Ile617Thr
XM_011510947.2:c.1790T>C	XP_011509249.1:p.Ile597Thr
XM_011510948.2:c.1724T>C	XP_011509250.1:p.Ile575Thr
XM_011510950.2:c.788T>C	XP_011509252.1:p.Ile263Thr
XM_017003789.1:c.1919T>C	XP_016859278.1:p.Ile640Thr
XR_001738696.1:n.1648T>C
XR_001738697.1:n.1645T>C
NM_015650.4:c.1820T>C MANE Select	NP_056465.2:p.Ile607Thr