Canonical Allele Identifier: CA67991006

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs185668144
• gnomAD v3: 2-238397675-C-G
• gnomAD v4: 2-238397675-C-G
• MyVariant Identifiers: chr2:g.239306316C>G (hg19) ; chr2:g.238397675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397675C>G , CM000664.2:g.238397675C>G	GRCh38
NC_000002.11:g.239306316C>G , CM000664.1:g.239306316C>G	GRCh37
NC_000002.10:g.238971055C>G	NCBI36
NG_053055.1:g.82187C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1906C>G MANE Select	ENSP00000362424.4:p.Gln636Glu
ENST00000373327.4:c.1906C>G	ENSP00000362424.4:p.Gln636Glu
ENST00000391993.7:c.1708C>G	ENSP00000375851.3:p.Gln570Glu
ENST00000462122.1:n.917C>G
ENST00000483951.1:n.254C>G
NM_001139490.1:c.1708C>G	NP_001132962.1:p.Gln570Glu
NM_015650.3:c.1906C>G	NP_056465.2:p.Gln636Glu
XM_006712414.1:c.1705C>G	XP_006712477.1:p.Gln569Glu
XM_011510944.1:c.2008C>G	XP_011509246.1:p.Gln670Glu
XM_011510945.1:c.1969C>G	XP_011509247.1:p.Gln657Glu
XM_011510946.1:c.1936C>G	XP_011509248.1:p.Gln646Glu
XM_011510947.1:c.1876C>G	XP_011509249.1:p.Gln626Glu
XM_011510948.1:c.1810C>G	XP_011509250.1:p.Gln604Glu
XM_011510950.1:c.874C>G	XP_011509252.1:p.Gln292Glu
XM_006712414.2:c.1705C>G	XP_006712477.1:p.Gln569Glu
XM_011510944.2:c.2008C>G	XP_011509246.1:p.Gln670Glu
XM_011510945.2:c.1969C>G	XP_011509247.1:p.Gln657Glu
XM_011510946.2:c.1936C>G	XP_011509248.1:p.Gln646Glu
XM_011510947.2:c.1876C>G	XP_011509249.1:p.Gln626Glu
XM_011510948.2:c.1810C>G	XP_011509250.1:p.Gln604Glu
XM_011510950.2:c.874C>G	XP_011509252.1:p.Gln292Glu
XM_017003789.1:c.2005C>G	XP_016859278.1:p.Gln669Glu
XR_001738696.1:n.1734C>G
XR_001738697.1:n.1731C>G
NM_015650.4:c.1906C>G MANE Select	NP_056465.2:p.Gln636Glu