Canonical Allele Identifier: CA351246811

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306304C>A (hg19) ; chr2:g.238397663C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397663C>A , CM000664.2:g.238397663C>A	GRCh38
NC_000002.11:g.239306304C>A , CM000664.1:g.239306304C>A	GRCh37
NC_000002.10:g.238971043C>A	NCBI36
NG_053055.1:g.82175C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1894C>A MANE Select	ENSP00000362424.4:p.Leu632Met
ENST00000373327.4:c.1894C>A	ENSP00000362424.4:p.Leu632Met
ENST00000391993.7:c.1696C>A	ENSP00000375851.3:p.Leu566Met
ENST00000462122.1:n.905C>A
ENST00000483951.1:n.242C>A
NM_001139490.1:c.1696C>A	NP_001132962.1:p.Leu566Met
NM_015650.3:c.1894C>A	NP_056465.2:p.Leu632Met
XM_006712414.1:c.1693C>A	XP_006712477.1:p.Leu565Met
XM_011510944.1:c.1996C>A	XP_011509246.1:p.Leu666Met
XM_011510945.1:c.1957C>A	XP_011509247.1:p.Leu653Met
XM_011510946.1:c.1924C>A	XP_011509248.1:p.Leu642Met
XM_011510947.1:c.1864C>A	XP_011509249.1:p.Leu622Met
XM_011510948.1:c.1798C>A	XP_011509250.1:p.Leu600Met
XM_011510950.1:c.862C>A	XP_011509252.1:p.Leu288Met
XM_006712414.2:c.1693C>A	XP_006712477.1:p.Leu565Met
XM_011510944.2:c.1996C>A	XP_011509246.1:p.Leu666Met
XM_011510945.2:c.1957C>A	XP_011509247.1:p.Leu653Met
XM_011510946.2:c.1924C>A	XP_011509248.1:p.Leu642Met
XM_011510947.2:c.1864C>A	XP_011509249.1:p.Leu622Met
XM_011510948.2:c.1798C>A	XP_011509250.1:p.Leu600Met
XM_011510950.2:c.862C>A	XP_011509252.1:p.Leu288Met
XM_017003789.1:c.1993C>A	XP_016859278.1:p.Leu665Met
XR_001738696.1:n.1722C>A
XR_001738697.1:n.1719C>A
NM_015650.4:c.1894C>A MANE Select	NP_056465.2:p.Leu632Met