Canonical Allele Identifier: CA351246845

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs1701294476
• MyVariant Identifiers: chr2:g.239306312G>T (hg19) ; chr2:g.238397671G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397671G>T , CM000664.2:g.238397671G>T	GRCh38
NC_000002.11:g.239306312G>T , CM000664.1:g.239306312G>T	GRCh37
NC_000002.10:g.238971051G>T	NCBI36
NG_053055.1:g.82183G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1902G>T MANE Select	ENSP00000362424.4:p.Gln634His
ENST00000373327.4:c.1902G>T	ENSP00000362424.4:p.Gln634His
ENST00000391993.7:c.1704G>T	ENSP00000375851.3:p.Gln568His
ENST00000462122.1:n.913G>T
ENST00000483951.1:n.250G>T
NM_001139490.1:c.1704G>T	NP_001132962.1:p.Gln568His
NM_015650.3:c.1902G>T	NP_056465.2:p.Gln634His
XM_006712414.1:c.1701G>T	XP_006712477.1:p.Gln567His
XM_011510944.1:c.2004G>T	XP_011509246.1:p.Gln668His
XM_011510945.1:c.1965G>T	XP_011509247.1:p.Gln655His
XM_011510946.1:c.1932G>T	XP_011509248.1:p.Gln644His
XM_011510947.1:c.1872G>T	XP_011509249.1:p.Gln624His
XM_011510948.1:c.1806G>T	XP_011509250.1:p.Gln602His
XM_011510950.1:c.870G>T	XP_011509252.1:p.Gln290His
XM_006712414.2:c.1701G>T	XP_006712477.1:p.Gln567His
XM_011510944.2:c.2004G>T	XP_011509246.1:p.Gln668His
XM_011510945.2:c.1965G>T	XP_011509247.1:p.Gln655His
XM_011510946.2:c.1932G>T	XP_011509248.1:p.Gln644His
XM_011510947.2:c.1872G>T	XP_011509249.1:p.Gln624His
XM_011510948.2:c.1806G>T	XP_011509250.1:p.Gln602His
XM_011510950.2:c.870G>T	XP_011509252.1:p.Gln290His
XM_017003789.1:c.2001G>T	XP_016859278.1:p.Gln667His
XR_001738696.1:n.1730G>T
XR_001738697.1:n.1727G>T
NM_015650.4:c.1902G>T MANE Select	NP_056465.2:p.Gln634His