Canonical Allele Identifier: CA351246631

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306274C>A (hg19) ; chr2:g.238397633C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397633C>A , CM000664.2:g.238397633C>A	GRCh38
NC_000002.11:g.239306274C>A , CM000664.1:g.239306274C>A	GRCh37
NC_000002.10:g.238971013C>A	NCBI36
NG_053055.1:g.82145C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373327.5:c.1864C>A MANE Select	ENSP00000362424.4:p.His622Asn
ENST00000373327.4:c.1864C>A	ENSP00000362424.4:p.His622Asn
ENST00000391993.7:c.1666C>A	ENSP00000375851.3:p.His556Asn
ENST00000462122.1:n.875C>A
ENST00000483951.1:n.212C>A
NM_001139490.1:c.1666C>A	NP_001132962.1:p.His556Asn
NM_015650.3:c.1864C>A	NP_056465.2:p.His622Asn
XM_006712414.1:c.1663C>A	XP_006712477.1:p.His555Asn
XM_011510944.1:c.1966C>A	XP_011509246.1:p.His656Asn
XM_011510945.1:c.1927C>A	XP_011509247.1:p.His643Asn
XM_011510946.1:c.1894C>A	XP_011509248.1:p.His632Asn
XM_011510947.1:c.1834C>A	XP_011509249.1:p.His612Asn
XM_011510948.1:c.1768C>A	XP_011509250.1:p.His590Asn
XM_011510950.1:c.832C>A	XP_011509252.1:p.His278Asn
XM_006712414.2:c.1663C>A	XP_006712477.1:p.His555Asn
XM_011510944.2:c.1966C>A	XP_011509246.1:p.His656Asn
XM_011510945.2:c.1927C>A	XP_011509247.1:p.His643Asn
XM_011510946.2:c.1894C>A	XP_011509248.1:p.His632Asn
XM_011510947.2:c.1834C>A	XP_011509249.1:p.His612Asn
XM_011510948.2:c.1768C>A	XP_011509250.1:p.His590Asn
XM_011510950.2:c.832C>A	XP_011509252.1:p.His278Asn
XM_017003789.1:c.1963C>A	XP_016859278.1:p.His655Asn
XR_001738696.1:n.1692C>A
XR_001738697.1:n.1689C>A
NM_015650.4:c.1864C>A MANE Select	NP_056465.2:p.His622Asn