Canonical Allele Identifier: CA351245868

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306146T>G (hg19) ; chr2:g.238397505T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397505T>G , CM000664.2:g.238397505T>G	GRCh38
NC_000002.11:g.239306146T>G , CM000664.1:g.239306146T>G	GRCh37
NC_000002.10:g.238970885T>G	NCBI36
NG_053055.1:g.82017T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1736T>G MANE Select	ENSP00000362424.4:p.Val579Gly
ENST00000373327.4:c.1736T>G	ENSP00000362424.4:p.Val579Gly
ENST00000391993.7:c.1538T>G	ENSP00000375851.3:p.Val513Gly
ENST00000462122.1:n.747T>G
ENST00000483951.1:n.84T>G
NM_001139490.1:c.1538T>G	NP_001132962.1:p.Val513Gly
NM_015650.3:c.1736T>G	NP_056465.2:p.Val579Gly
XM_006712414.1:c.1535T>G	XP_006712477.1:p.Val512Gly
XM_011510944.1:c.1838T>G	XP_011509246.1:p.Val613Gly
XM_011510945.1:c.1799T>G	XP_011509247.1:p.Val600Gly
XM_011510946.1:c.1766T>G	XP_011509248.1:p.Val589Gly
XM_011510947.1:c.1706T>G	XP_011509249.1:p.Val569Gly
XM_011510948.1:c.1640T>G	XP_011509250.1:p.Val547Gly
XM_011510950.1:c.704T>G	XP_011509252.1:p.Val235Gly
XR_922902.1:n.2035T>G
XM_006712414.2:c.1535T>G	XP_006712477.1:p.Val512Gly
XM_011510944.2:c.1838T>G	XP_011509246.1:p.Val613Gly
XM_011510945.2:c.1799T>G	XP_011509247.1:p.Val600Gly
XM_011510946.2:c.1766T>G	XP_011509248.1:p.Val589Gly
XM_011510947.2:c.1706T>G	XP_011509249.1:p.Val569Gly
XM_011510948.2:c.1640T>G	XP_011509250.1:p.Val547Gly
XM_011510950.2:c.704T>G	XP_011509252.1:p.Val235Gly
XM_017003789.1:c.1835T>G	XP_016859278.1:p.Val612Gly
XR_001738696.1:n.1564T>G
XR_001738697.1:n.1561T>G
XR_922902.2:n.2098T>G
NM_015650.4:c.1736T>G MANE Select	NP_056465.2:p.Val579Gly