Canonical Allele Identifier: CA351245988

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306173C>G (hg19) ; chr2:g.238397532C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397532C>G , CM000664.2:g.238397532C>G	GRCh38
NC_000002.11:g.239306173C>G , CM000664.1:g.239306173C>G	GRCh37
NC_000002.10:g.238970912C>G	NCBI36
NG_053055.1:g.82044C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1763C>G MANE Select	ENSP00000362424.4:p.Thr588Arg
ENST00000373327.4:c.1763C>G	ENSP00000362424.4:p.Thr588Arg
ENST00000391993.7:c.1565C>G	ENSP00000375851.3:p.Thr522Arg
ENST00000462122.1:n.774C>G
ENST00000483951.1:n.111C>G
NM_001139490.1:c.1565C>G	NP_001132962.1:p.Thr522Arg
NM_015650.3:c.1763C>G	NP_056465.2:p.Thr588Arg
XM_006712414.1:c.1562C>G	XP_006712477.1:p.Thr521Arg
XM_011510944.1:c.1865C>G	XP_011509246.1:p.Thr622Arg
XM_011510945.1:c.1826C>G	XP_011509247.1:p.Thr609Arg
XM_011510946.1:c.1793C>G	XP_011509248.1:p.Thr598Arg
XM_011510947.1:c.1733C>G	XP_011509249.1:p.Thr578Arg
XM_011510948.1:c.1667C>G	XP_011509250.1:p.Thr556Arg
XM_011510950.1:c.731C>G	XP_011509252.1:p.Thr244Arg
XR_922902.1:n.2062C>G
XM_006712414.2:c.1562C>G	XP_006712477.1:p.Thr521Arg
XM_011510944.2:c.1865C>G	XP_011509246.1:p.Thr622Arg
XM_011510945.2:c.1826C>G	XP_011509247.1:p.Thr609Arg
XM_011510946.2:c.1793C>G	XP_011509248.1:p.Thr598Arg
XM_011510947.2:c.1733C>G	XP_011509249.1:p.Thr578Arg
XM_011510948.2:c.1667C>G	XP_011509250.1:p.Thr556Arg
XM_011510950.2:c.731C>G	XP_011509252.1:p.Thr244Arg
XM_017003789.1:c.1862C>G	XP_016859278.1:p.Thr621Arg
XR_001738696.1:n.1591C>G
XR_001738697.1:n.1588C>G
NM_015650.4:c.1763C>G MANE Select	NP_056465.2:p.Thr588Arg