Canonical Allele Identifier: CA351246777

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306296C>A (hg19) ; chr2:g.238397655C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397655C>A , CM000664.2:g.238397655C>A	GRCh38
NC_000002.11:g.239306296C>A , CM000664.1:g.239306296C>A	GRCh37
NC_000002.10:g.238971035C>A	NCBI36
NG_053055.1:g.82167C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1886C>A MANE Select	ENSP00000362424.4:p.Ala629Asp
ENST00000373327.4:c.1886C>A	ENSP00000362424.4:p.Ala629Asp
ENST00000391993.7:c.1688C>A	ENSP00000375851.3:p.Ala563Asp
ENST00000462122.1:n.897C>A
ENST00000483951.1:n.234C>A
NM_001139490.1:c.1688C>A	NP_001132962.1:p.Ala563Asp
NM_015650.3:c.1886C>A	NP_056465.2:p.Ala629Asp
XM_006712414.1:c.1685C>A	XP_006712477.1:p.Ala562Asp
XM_011510944.1:c.1988C>A	XP_011509246.1:p.Ala663Asp
XM_011510945.1:c.1949C>A	XP_011509247.1:p.Ala650Asp
XM_011510946.1:c.1916C>A	XP_011509248.1:p.Ala639Asp
XM_011510947.1:c.1856C>A	XP_011509249.1:p.Ala619Asp
XM_011510948.1:c.1790C>A	XP_011509250.1:p.Ala597Asp
XM_011510950.1:c.854C>A	XP_011509252.1:p.Ala285Asp
XM_006712414.2:c.1685C>A	XP_006712477.1:p.Ala562Asp
XM_011510944.2:c.1988C>A	XP_011509246.1:p.Ala663Asp
XM_011510945.2:c.1949C>A	XP_011509247.1:p.Ala650Asp
XM_011510946.2:c.1916C>A	XP_011509248.1:p.Ala639Asp
XM_011510947.2:c.1856C>A	XP_011509249.1:p.Ala619Asp
XM_011510948.2:c.1790C>A	XP_011509250.1:p.Ala597Asp
XM_011510950.2:c.854C>A	XP_011509252.1:p.Ala285Asp
XM_017003789.1:c.1985C>A	XP_016859278.1:p.Ala662Asp
XR_001738696.1:n.1714C>A
XR_001738697.1:n.1711C>A
NM_015650.4:c.1886C>A MANE Select	NP_056465.2:p.Ala629Asp