Canonical Allele Identifier: CA351246593

Gene: TRAF3IP1

Linked Data

• gnomAD v4: 2-238397627-A-G
• MyVariant Identifiers: chr2:g.239306268A>G (hg19) ; chr2:g.238397627A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1858A>G MANE Select	ENSP00000362424.4:p.Met620Val
ENST00000373327.4:c.1858A>G	ENSP00000362424.4:p.Met620Val
ENST00000391993.7:c.1660A>G	ENSP00000375851.3:p.Met554Val
ENST00000462122.1:n.869A>G
ENST00000483951.1:n.206A>G
NM_001139490.1:c.1660A>G	NP_001132962.1:p.Met554Val
NM_015650.3:c.1858A>G	NP_056465.2:p.Met620Val
XM_006712414.1:c.1657A>G	XP_006712477.1:p.Met553Val
XM_011510944.1:c.1960A>G	XP_011509246.1:p.Met654Val
XM_011510945.1:c.1921A>G	XP_011509247.1:p.Met641Val
XM_011510946.1:c.1888A>G	XP_011509248.1:p.Met630Val
XM_011510947.1:c.1828A>G	XP_011509249.1:p.Met610Val
XM_011510948.1:c.1762A>G	XP_011509250.1:p.Met588Val
XM_011510950.1:c.826A>G	XP_011509252.1:p.Met276Val
XM_006712414.2:c.1657A>G	XP_006712477.1:p.Met553Val
XM_011510944.2:c.1960A>G	XP_011509246.1:p.Met654Val
XM_011510945.2:c.1921A>G	XP_011509247.1:p.Met641Val
XM_011510946.2:c.1888A>G	XP_011509248.1:p.Met630Val
XM_011510947.2:c.1828A>G	XP_011509249.1:p.Met610Val
XM_011510948.2:c.1762A>G	XP_011509250.1:p.Met588Val
XM_011510950.2:c.826A>G	XP_011509252.1:p.Met276Val
XM_017003789.1:c.1957A>G	XP_016859278.1:p.Met653Val
XR_001738696.1:n.1686A>G
XR_001738697.1:n.1683A>G
NM_015650.4:c.1858A>G MANE Select	NP_056465.2:p.Met620Val