Canonical Allele Identifier: CA1338105481

Gene: TRAF3IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397627A= , CM000664.2:g.238397627A=	GRCh38
NC_000002.11:g.239306268A= , CM000664.1:g.239306268A=	GRCh37
NC_000002.10:g.238971007A=	NCBI36
NG_053055.1:g.82139A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373327.5:c.1858A= MANE Select	ENSP00000362424.4:p.Met620=
ENST00000373327.4:c.1858A=	ENSP00000362424.4:p.Met620=
ENST00000391993.7:c.1660A=	ENSP00000375851.3:p.Met554=
ENST00000462122.1:n.869A=
ENST00000483951.1:n.206A=
NM_001139490.1:c.1660A=	NP_001132962.1:p.Met554=
NM_015650.3:c.1858A=	NP_056465.2:p.Met620=
XM_006712414.1:c.1657A=	XP_006712477.1:p.Met553=
XM_011510944.1:c.1960A=	XP_011509246.1:p.Met654=
XM_011510945.1:c.1921A=	XP_011509247.1:p.Met641=
XM_011510946.1:c.1888A=	XP_011509248.1:p.Met630=
XM_011510947.1:c.1828A=	XP_011509249.1:p.Met610=
XM_011510948.1:c.1762A=	XP_011509250.1:p.Met588=
XM_011510950.1:c.826A=	XP_011509252.1:p.Met276=
XM_006712414.2:c.1657A=	XP_006712477.1:p.Met553=
XM_011510944.2:c.1960A=	XP_011509246.1:p.Met654=
XM_011510945.2:c.1921A=	XP_011509247.1:p.Met641=
XM_011510946.2:c.1888A=	XP_011509248.1:p.Met630=
XM_011510947.2:c.1828A=	XP_011509249.1:p.Met610=
XM_011510948.2:c.1762A=	XP_011509250.1:p.Met588=
XM_011510950.2:c.826A=	XP_011509252.1:p.Met276=
XM_017003789.1:c.1957A=	XP_016859278.1:p.Met653=
XR_001738696.1:n.1686A=
XR_001738697.1:n.1683A=
NM_015650.4:c.1858A= MANE Select	NP_056465.2:p.Met620=