Canonical Allele Identifier: CA351246294

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306223G>C (hg19) ; chr2:g.238397582G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397582G>C , CM000664.2:g.238397582G>C	GRCh38
NC_000002.11:g.239306223G>C , CM000664.1:g.239306223G>C	GRCh37
NC_000002.10:g.238970962G>C	NCBI36
NG_053055.1:g.82094G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1813G>C MANE Select	ENSP00000362424.4:p.Asp605His
ENST00000373327.4:c.1813G>C	ENSP00000362424.4:p.Asp605His
ENST00000391993.7:c.1615G>C	ENSP00000375851.3:p.Asp539His
ENST00000462122.1:n.824G>C
ENST00000483951.1:n.161G>C
NM_001139490.1:c.1615G>C	NP_001132962.1:p.Asp539His
NM_015650.3:c.1813G>C	NP_056465.2:p.Asp605His
XM_006712414.1:c.1612G>C	XP_006712477.1:p.Asp538His
XM_011510944.1:c.1915G>C	XP_011509246.1:p.Asp639His
XM_011510945.1:c.1876G>C	XP_011509247.1:p.Asp626His
XM_011510946.1:c.1843G>C	XP_011509248.1:p.Asp615His
XM_011510947.1:c.1783G>C	XP_011509249.1:p.Asp595His
XM_011510948.1:c.1717G>C	XP_011509250.1:p.Asp573His
XM_011510950.1:c.781G>C	XP_011509252.1:p.Asp261His
XM_006712414.2:c.1612G>C	XP_006712477.1:p.Asp538His
XM_011510944.2:c.1915G>C	XP_011509246.1:p.Asp639His
XM_011510945.2:c.1876G>C	XP_011509247.1:p.Asp626His
XM_011510946.2:c.1843G>C	XP_011509248.1:p.Asp615His
XM_011510947.2:c.1783G>C	XP_011509249.1:p.Asp595His
XM_011510948.2:c.1717G>C	XP_011509250.1:p.Asp573His
XM_011510950.2:c.781G>C	XP_011509252.1:p.Asp261His
XM_017003789.1:c.1912G>C	XP_016859278.1:p.Asp638His
XR_001738696.1:n.1641G>C
XR_001738697.1:n.1638G>C
NM_015650.4:c.1813G>C MANE Select	NP_056465.2:p.Asp605His