Canonical Allele Identifier: CA432228069

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306105A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397464A>G , CM000664.2:g.238397464A>G	GRCh38
NC_000002.11:g.239306105A>G , CM000664.1:g.239306105A>G	GRCh37
NC_000002.10:g.238970844A>G	NCBI36
NG_053055.1:g.81976A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1695A>G MANE Select	ENSP00000362424.4:p.Arg565=
ENST00000373327.4:c.1695A>G	ENSP00000362424.4:p.Arg565=
ENST00000391993.7:c.1497A>G	ENSP00000375851.3:p.Arg499=
ENST00000462122.1:n.706A>G
ENST00000483951.1:n.43A>G
NM_001139490.1:c.1497A>G	NP_001132962.1:p.Arg499=
NM_015650.3:c.1695A>G	NP_056465.2:p.Arg565=
XM_006712414.1:c.1494A>G	XP_006712477.1:p.Arg498=
XM_011510944.1:c.1797A>G	XP_011509246.1:p.Arg599=
XM_011510945.1:c.1758A>G	XP_011509247.1:p.Arg586=
XM_011510946.1:c.1725A>G	XP_011509248.1:p.Arg575=
XM_011510947.1:c.1665A>G	XP_011509249.1:p.Arg555=
XM_011510948.1:c.1599A>G	XP_011509250.1:p.Arg533=
XM_011510950.1:c.663A>G	XP_011509252.1:p.Arg221=
XR_922902.1:n.1994A>G
XM_006712414.2:c.1494A>G	XP_006712477.1:p.Arg498=
XM_011510944.2:c.1797A>G	XP_011509246.1:p.Arg599=
XM_011510945.2:c.1758A>G	XP_011509247.1:p.Arg586=
XM_011510946.2:c.1725A>G	XP_011509248.1:p.Arg575=
XM_011510947.2:c.1665A>G	XP_011509249.1:p.Arg555=
XM_011510948.2:c.1599A>G	XP_011509250.1:p.Arg533=
XM_011510950.2:c.663A>G	XP_011509252.1:p.Arg221=
XM_017003789.1:c.1794A>G	XP_016859278.1:p.Arg598=
XR_001738696.1:n.1523A>G
XR_001738697.1:n.1520A>G
XR_922902.2:n.2057A>G
NM_015650.4:c.1695A>G MANE Select	NP_056465.2:p.Arg565=