Canonical Allele Identifier: CA432228099

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306168C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397527C>G , CM000664.2:g.238397527C>G	GRCh38
NC_000002.11:g.239306168C>G , CM000664.1:g.239306168C>G	GRCh37
NC_000002.10:g.238970907C>G	NCBI36
NG_053055.1:g.82039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1758C>G MANE Select	ENSP00000362424.4:p.Leu586=
ENST00000373327.4:c.1758C>G	ENSP00000362424.4:p.Leu586=
ENST00000391993.7:c.1560C>G	ENSP00000375851.3:p.Leu520=
ENST00000462122.1:n.769C>G
ENST00000483951.1:n.106C>G
NM_001139490.1:c.1560C>G	NP_001132962.1:p.Leu520=
NM_015650.3:c.1758C>G	NP_056465.2:p.Leu586=
XM_006712414.1:c.1557C>G	XP_006712477.1:p.Leu519=
XM_011510944.1:c.1860C>G	XP_011509246.1:p.Leu620=
XM_011510945.1:c.1821C>G	XP_011509247.1:p.Leu607=
XM_011510946.1:c.1788C>G	XP_011509248.1:p.Leu596=
XM_011510947.1:c.1728C>G	XP_011509249.1:p.Leu576=
XM_011510948.1:c.1662C>G	XP_011509250.1:p.Leu554=
XM_011510950.1:c.726C>G	XP_011509252.1:p.Leu242=
XR_922902.1:n.2057C>G
XM_006712414.2:c.1557C>G	XP_006712477.1:p.Leu519=
XM_011510944.2:c.1860C>G	XP_011509246.1:p.Leu620=
XM_011510945.2:c.1821C>G	XP_011509247.1:p.Leu607=
XM_011510946.2:c.1788C>G	XP_011509248.1:p.Leu596=
XM_011510947.2:c.1728C>G	XP_011509249.1:p.Leu576=
XM_011510948.2:c.1662C>G	XP_011509250.1:p.Leu554=
XM_011510950.2:c.726C>G	XP_011509252.1:p.Leu242=
XM_017003789.1:c.1857C>G	XP_016859278.1:p.Leu619=
XR_001738696.1:n.1586C>G
XR_001738697.1:n.1583C>G
NM_015650.4:c.1758C>G MANE Select	NP_056465.2:p.Leu586=