Canonical Allele Identifier: CA351246552

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306261G>T (hg19) ; chr2:g.238397620G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397620G>T , CM000664.2:g.238397620G>T	GRCh38
NC_000002.11:g.239306261G>T , CM000664.1:g.239306261G>T	GRCh37
NC_000002.10:g.238971000G>T	NCBI36
NG_053055.1:g.82132G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1851G>T MANE Select	ENSP00000362424.4:p.Glu617Asp
ENST00000373327.4:c.1851G>T	ENSP00000362424.4:p.Glu617Asp
ENST00000391993.7:c.1653G>T	ENSP00000375851.3:p.Glu551Asp
ENST00000462122.1:n.862G>T
ENST00000483951.1:n.199G>T
NM_001139490.1:c.1653G>T	NP_001132962.1:p.Glu551Asp
NM_015650.3:c.1851G>T	NP_056465.2:p.Glu617Asp
XM_006712414.1:c.1650G>T	XP_006712477.1:p.Glu550Asp
XM_011510944.1:c.1953G>T	XP_011509246.1:p.Glu651Asp
XM_011510945.1:c.1914G>T	XP_011509247.1:p.Glu638Asp
XM_011510946.1:c.1881G>T	XP_011509248.1:p.Glu627Asp
XM_011510947.1:c.1821G>T	XP_011509249.1:p.Glu607Asp
XM_011510948.1:c.1755G>T	XP_011509250.1:p.Glu585Asp
XM_011510950.1:c.819G>T	XP_011509252.1:p.Glu273Asp
XM_006712414.2:c.1650G>T	XP_006712477.1:p.Glu550Asp
XM_011510944.2:c.1953G>T	XP_011509246.1:p.Glu651Asp
XM_011510945.2:c.1914G>T	XP_011509247.1:p.Glu638Asp
XM_011510946.2:c.1881G>T	XP_011509248.1:p.Glu627Asp
XM_011510947.2:c.1821G>T	XP_011509249.1:p.Glu607Asp
XM_011510948.2:c.1755G>T	XP_011509250.1:p.Glu585Asp
XM_011510950.2:c.819G>T	XP_011509252.1:p.Glu273Asp
XM_017003789.1:c.1950G>T	XP_016859278.1:p.Glu650Asp
XR_001738696.1:n.1679G>T
XR_001738697.1:n.1676G>T
NM_015650.4:c.1851G>T MANE Select	NP_056465.2:p.Glu617Asp