Canonical Allele Identifier: CA351246285

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs199664401
• gnomAD v2: 2-239306221-T-C
• gnomAD v4: 2-238397580-T-C
• MyVariant Identifiers: chr2:g.239306221T>C (hg19) ; chr2:g.238397580T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397580T>C , CM000664.2:g.238397580T>C	GRCh38
NC_000002.11:g.239306221T>C , CM000664.1:g.239306221T>C	GRCh37
NC_000002.10:g.238970960T>C	NCBI36
NG_053055.1:g.82092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1811T>C MANE Select	ENSP00000362424.4:p.Met604Thr
ENST00000373327.4:c.1811T>C	ENSP00000362424.4:p.Met604Thr
ENST00000391993.7:c.1613T>C	ENSP00000375851.3:p.Met538Thr
ENST00000462122.1:n.822T>C
ENST00000483951.1:n.159T>C
NM_001139490.1:c.1613T>C	NP_001132962.1:p.Met538Thr
NM_015650.3:c.1811T>C	NP_056465.2:p.Met604Thr
XM_006712414.1:c.1610T>C	XP_006712477.1:p.Met537Thr
XM_011510944.1:c.1913T>C	XP_011509246.1:p.Met638Thr
XM_011510945.1:c.1874T>C	XP_011509247.1:p.Met625Thr
XM_011510946.1:c.1841T>C	XP_011509248.1:p.Met614Thr
XM_011510947.1:c.1781T>C	XP_011509249.1:p.Met594Thr
XM_011510948.1:c.1715T>C	XP_011509250.1:p.Met572Thr
XM_011510950.1:c.779T>C	XP_011509252.1:p.Met260Thr
XM_006712414.2:c.1610T>C	XP_006712477.1:p.Met537Thr
XM_011510944.2:c.1913T>C	XP_011509246.1:p.Met638Thr
XM_011510945.2:c.1874T>C	XP_011509247.1:p.Met625Thr
XM_011510946.2:c.1841T>C	XP_011509248.1:p.Met614Thr
XM_011510947.2:c.1781T>C	XP_011509249.1:p.Met594Thr
XM_011510948.2:c.1715T>C	XP_011509250.1:p.Met572Thr
XM_011510950.2:c.779T>C	XP_011509252.1:p.Met260Thr
XM_017003789.1:c.1910T>C	XP_016859278.1:p.Met637Thr
XR_001738696.1:n.1639T>C
XR_001738697.1:n.1636T>C
NM_015650.4:c.1811T>C MANE Select	NP_056465.2:p.Met604Thr