Canonical Allele Identifier: CA351245890

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs769447347
• gnomAD v3: 2-238397512-G-C
• gnomAD v4: 2-238397512-G-C
• MyVariant Identifiers: chr2:g.239306153G>C (hg19) ; chr2:g.238397512G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397512G>C , CM000664.2:g.238397512G>C	GRCh38
NC_000002.11:g.239306153G>C , CM000664.1:g.239306153G>C	GRCh37
NC_000002.10:g.238970892G>C	NCBI36
NG_053055.1:g.82024G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1743G>C MANE Select	ENSP00000362424.4:p.Lys581Asn
ENST00000373327.4:c.1743G>C	ENSP00000362424.4:p.Lys581Asn
ENST00000391993.7:c.1545G>C	ENSP00000375851.3:p.Lys515Asn
ENST00000462122.1:n.754G>C
ENST00000483951.1:n.91G>C
NM_001139490.1:c.1545G>C	NP_001132962.1:p.Lys515Asn
NM_015650.3:c.1743G>C	NP_056465.2:p.Lys581Asn
XM_006712414.1:c.1542G>C	XP_006712477.1:p.Lys514Asn
XM_011510944.1:c.1845G>C	XP_011509246.1:p.Lys615Asn
XM_011510945.1:c.1806G>C	XP_011509247.1:p.Lys602Asn
XM_011510946.1:c.1773G>C	XP_011509248.1:p.Lys591Asn
XM_011510947.1:c.1713G>C	XP_011509249.1:p.Lys571Asn
XM_011510948.1:c.1647G>C	XP_011509250.1:p.Lys549Asn
XM_011510950.1:c.711G>C	XP_011509252.1:p.Lys237Asn
XR_922902.1:n.2042G>C
XM_006712414.2:c.1542G>C	XP_006712477.1:p.Lys514Asn
XM_011510944.2:c.1845G>C	XP_011509246.1:p.Lys615Asn
XM_011510945.2:c.1806G>C	XP_011509247.1:p.Lys602Asn
XM_011510946.2:c.1773G>C	XP_011509248.1:p.Lys591Asn
XM_011510947.2:c.1713G>C	XP_011509249.1:p.Lys571Asn
XM_011510948.2:c.1647G>C	XP_011509250.1:p.Lys549Asn
XM_011510950.2:c.711G>C	XP_011509252.1:p.Lys237Asn
XM_017003789.1:c.1842G>C	XP_016859278.1:p.Lys614Asn
XR_001738696.1:n.1571G>C
XR_001738697.1:n.1568G>C
XR_922902.2:n.2105G>C
NM_015650.4:c.1743G>C MANE Select	NP_056465.2:p.Lys581Asn