Canonical Allele Identifier: CA351246043

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306181C>G (hg19) ; chr2:g.238397540C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397540C>G , CM000664.2:g.238397540C>G	GRCh38
NC_000002.11:g.239306181C>G , CM000664.1:g.239306181C>G	GRCh37
NC_000002.10:g.238970920C>G	NCBI36
NG_053055.1:g.82052C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1771C>G MANE Select	ENSP00000362424.4:p.Gln591Glu
ENST00000373327.4:c.1771C>G	ENSP00000362424.4:p.Gln591Glu
ENST00000391993.7:c.1573C>G	ENSP00000375851.3:p.Gln525Glu
ENST00000462122.1:n.782C>G
ENST00000483951.1:n.119C>G
NM_001139490.1:c.1573C>G	NP_001132962.1:p.Gln525Glu
NM_015650.3:c.1771C>G	NP_056465.2:p.Gln591Glu
XM_006712414.1:c.1570C>G	XP_006712477.1:p.Gln524Glu
XM_011510944.1:c.1873C>G	XP_011509246.1:p.Gln625Glu
XM_011510945.1:c.1834C>G	XP_011509247.1:p.Gln612Glu
XM_011510946.1:c.1801C>G	XP_011509248.1:p.Gln601Glu
XM_011510947.1:c.1741C>G	XP_011509249.1:p.Gln581Glu
XM_011510948.1:c.1675C>G	XP_011509250.1:p.Gln559Glu
XM_011510950.1:c.739C>G	XP_011509252.1:p.Gln247Glu
XM_006712414.2:c.1570C>G	XP_006712477.1:p.Gln524Glu
XM_011510944.2:c.1873C>G	XP_011509246.1:p.Gln625Glu
XM_011510945.2:c.1834C>G	XP_011509247.1:p.Gln612Glu
XM_011510946.2:c.1801C>G	XP_011509248.1:p.Gln601Glu
XM_011510947.2:c.1741C>G	XP_011509249.1:p.Gln581Glu
XM_011510948.2:c.1675C>G	XP_011509250.1:p.Gln559Glu
XM_011510950.2:c.739C>G	XP_011509252.1:p.Gln247Glu
XM_017003789.1:c.1870C>G	XP_016859278.1:p.Gln624Glu
XR_001738696.1:n.1599C>G
XR_001738697.1:n.1596C>G
NM_015650.4:c.1771C>G MANE Select	NP_056465.2:p.Gln591Glu