Canonical Allele Identifier: CA351246601

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306269T>G (hg19) ; chr2:g.238397628T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397628T>G , CM000664.2:g.238397628T>G	GRCh38
NC_000002.11:g.239306269T>G , CM000664.1:g.239306269T>G	GRCh37
NC_000002.10:g.238971008T>G	NCBI36
NG_053055.1:g.82140T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1859T>G MANE Select	ENSP00000362424.4:p.Met620Arg
ENST00000373327.4:c.1859T>G	ENSP00000362424.4:p.Met620Arg
ENST00000391993.7:c.1661T>G	ENSP00000375851.3:p.Met554Arg
ENST00000462122.1:n.870T>G
ENST00000483951.1:n.207T>G
NM_001139490.1:c.1661T>G	NP_001132962.1:p.Met554Arg
NM_015650.3:c.1859T>G	NP_056465.2:p.Met620Arg
XM_006712414.1:c.1658T>G	XP_006712477.1:p.Met553Arg
XM_011510944.1:c.1961T>G	XP_011509246.1:p.Met654Arg
XM_011510945.1:c.1922T>G	XP_011509247.1:p.Met641Arg
XM_011510946.1:c.1889T>G	XP_011509248.1:p.Met630Arg
XM_011510947.1:c.1829T>G	XP_011509249.1:p.Met610Arg
XM_011510948.1:c.1763T>G	XP_011509250.1:p.Met588Arg
XM_011510950.1:c.827T>G	XP_011509252.1:p.Met276Arg
XM_006712414.2:c.1658T>G	XP_006712477.1:p.Met553Arg
XM_011510944.2:c.1961T>G	XP_011509246.1:p.Met654Arg
XM_011510945.2:c.1922T>G	XP_011509247.1:p.Met641Arg
XM_011510946.2:c.1889T>G	XP_011509248.1:p.Met630Arg
XM_011510947.2:c.1829T>G	XP_011509249.1:p.Met610Arg
XM_011510948.2:c.1763T>G	XP_011509250.1:p.Met588Arg
XM_011510950.2:c.827T>G	XP_011509252.1:p.Met276Arg
XM_017003789.1:c.1958T>G	XP_016859278.1:p.Met653Arg
XR_001738696.1:n.1687T>G
XR_001738697.1:n.1684T>G
NM_015650.4:c.1859T>G MANE Select	NP_056465.2:p.Met620Arg