Canonical Allele Identifier: CA432228362

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306303C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397662C>A , CM000664.2:g.238397662C>A	GRCh38
NC_000002.11:g.239306303C>A , CM000664.1:g.239306303C>A	GRCh37
NC_000002.10:g.238971042C>A	NCBI36
NG_053055.1:g.82174C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1893C>A MANE Select	ENSP00000362424.4:p.Ala631=
ENST00000373327.4:c.1893C>A	ENSP00000362424.4:p.Ala631=
ENST00000391993.7:c.1695C>A	ENSP00000375851.3:p.Ala565=
ENST00000462122.1:n.904C>A
ENST00000483951.1:n.241C>A
NM_001139490.1:c.1695C>A	NP_001132962.1:p.Ala565=
NM_015650.3:c.1893C>A	NP_056465.2:p.Ala631=
XM_006712414.1:c.1692C>A	XP_006712477.1:p.Ala564=
XM_011510944.1:c.1995C>A	XP_011509246.1:p.Ala665=
XM_011510945.1:c.1956C>A	XP_011509247.1:p.Ala652=
XM_011510946.1:c.1923C>A	XP_011509248.1:p.Ala641=
XM_011510947.1:c.1863C>A	XP_011509249.1:p.Ala621=
XM_011510948.1:c.1797C>A	XP_011509250.1:p.Ala599=
XM_011510950.1:c.861C>A	XP_011509252.1:p.Ala287=
XM_006712414.2:c.1692C>A	XP_006712477.1:p.Ala564=
XM_011510944.2:c.1995C>A	XP_011509246.1:p.Ala665=
XM_011510945.2:c.1956C>A	XP_011509247.1:p.Ala652=
XM_011510946.2:c.1923C>A	XP_011509248.1:p.Ala641=
XM_011510947.2:c.1863C>A	XP_011509249.1:p.Ala621=
XM_011510948.2:c.1797C>A	XP_011509250.1:p.Ala599=
XM_011510950.2:c.861C>A	XP_011509252.1:p.Ala287=
XM_017003789.1:c.1992C>A	XP_016859278.1:p.Ala664=
XR_001738696.1:n.1721C>A
XR_001738697.1:n.1718C>A
NM_015650.4:c.1893C>A MANE Select	NP_056465.2:p.Ala631=