Canonical Allele Identifier: CA351246527

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306257A>T (hg19) ; chr2:g.238397616A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397616A>T , CM000664.2:g.238397616A>T	GRCh38
NC_000002.11:g.239306257A>T , CM000664.1:g.239306257A>T	GRCh37
NC_000002.10:g.238970996A>T	NCBI36
NG_053055.1:g.82128A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1847A>T MANE Select	ENSP00000362424.4:p.Asn616Ile
ENST00000373327.4:c.1847A>T	ENSP00000362424.4:p.Asn616Ile
ENST00000391993.7:c.1649A>T	ENSP00000375851.3:p.Asn550Ile
ENST00000462122.1:n.858A>T
ENST00000483951.1:n.195A>T
NM_001139490.1:c.1649A>T	NP_001132962.1:p.Asn550Ile
NM_015650.3:c.1847A>T	NP_056465.2:p.Asn616Ile
XM_006712414.1:c.1646A>T	XP_006712477.1:p.Asn549Ile
XM_011510944.1:c.1949A>T	XP_011509246.1:p.Asn650Ile
XM_011510945.1:c.1910A>T	XP_011509247.1:p.Asn637Ile
XM_011510946.1:c.1877A>T	XP_011509248.1:p.Asn626Ile
XM_011510947.1:c.1817A>T	XP_011509249.1:p.Asn606Ile
XM_011510948.1:c.1751A>T	XP_011509250.1:p.Asn584Ile
XM_011510950.1:c.815A>T	XP_011509252.1:p.Asn272Ile
XM_006712414.2:c.1646A>T	XP_006712477.1:p.Asn549Ile
XM_011510944.2:c.1949A>T	XP_011509246.1:p.Asn650Ile
XM_011510945.2:c.1910A>T	XP_011509247.1:p.Asn637Ile
XM_011510946.2:c.1877A>T	XP_011509248.1:p.Asn626Ile
XM_011510947.2:c.1817A>T	XP_011509249.1:p.Asn606Ile
XM_011510948.2:c.1751A>T	XP_011509250.1:p.Asn584Ile
XM_011510950.2:c.815A>T	XP_011509252.1:p.Asn272Ile
XM_017003789.1:c.1946A>T	XP_016859278.1:p.Asn649Ile
XR_001738696.1:n.1675A>T
XR_001738697.1:n.1672A>T
NM_015650.4:c.1847A>T MANE Select	NP_056465.2:p.Asn616Ile