Canonical Allele Identifier: CA351246344

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306231C>G (hg19) ; chr2:g.238397590C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397590C>G , CM000664.2:g.238397590C>G	GRCh38
NC_000002.11:g.239306231C>G , CM000664.1:g.239306231C>G	GRCh37
NC_000002.10:g.238970970C>G	NCBI36
NG_053055.1:g.82102C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1821C>G MANE Select	ENSP00000362424.4:p.Ile607Met
ENST00000373327.4:c.1821C>G	ENSP00000362424.4:p.Ile607Met
ENST00000391993.7:c.1623C>G	ENSP00000375851.3:p.Ile541Met
ENST00000462122.1:n.832C>G
ENST00000483951.1:n.169C>G
NM_001139490.1:c.1623C>G	NP_001132962.1:p.Ile541Met
NM_015650.3:c.1821C>G	NP_056465.2:p.Ile607Met
XM_006712414.1:c.1620C>G	XP_006712477.1:p.Ile540Met
XM_011510944.1:c.1923C>G	XP_011509246.1:p.Ile641Met
XM_011510945.1:c.1884C>G	XP_011509247.1:p.Ile628Met
XM_011510946.1:c.1851C>G	XP_011509248.1:p.Ile617Met
XM_011510947.1:c.1791C>G	XP_011509249.1:p.Ile597Met
XM_011510948.1:c.1725C>G	XP_011509250.1:p.Ile575Met
XM_011510950.1:c.789C>G	XP_011509252.1:p.Ile263Met
XM_006712414.2:c.1620C>G	XP_006712477.1:p.Ile540Met
XM_011510944.2:c.1923C>G	XP_011509246.1:p.Ile641Met
XM_011510945.2:c.1884C>G	XP_011509247.1:p.Ile628Met
XM_011510946.2:c.1851C>G	XP_011509248.1:p.Ile617Met
XM_011510947.2:c.1791C>G	XP_011509249.1:p.Ile597Met
XM_011510948.2:c.1725C>G	XP_011509250.1:p.Ile575Met
XM_011510950.2:c.789C>G	XP_011509252.1:p.Ile263Met
XM_017003789.1:c.1920C>G	XP_016859278.1:p.Ile640Met
XR_001738696.1:n.1649C>G
XR_001738697.1:n.1646C>G
NM_015650.4:c.1821C>G MANE Select	NP_056465.2:p.Ile607Met