Canonical Allele Identifier: CA67990650

Gene: TRAF3IP1

Linked Data

• dbSNP Id: rs373569951
• gnomAD v4: 2-238397454-T-C
• MyVariant Identifiers: chr2:g.238397454T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397454T>C , CM000664.2:g.238397454T>C	GRCh38
NC_000002.11:g.239306095T>C , CM000664.1:g.239306095T>C	GRCh37
NC_000002.10:g.238970834T>C	NCBI36
NG_053055.1:g.81966T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1690-5T>C MANE Select	ENSP00000362424.4:n.1690-5T>C
ENST00000373327.4:c.1690-5T>C	ENSP00000362424.4:n.1690-5T>C
ENST00000391993.7:c.1492-5T>C	ENSP00000375851.3:n.1492-5T>C
ENST00000462122.1:n.701-5T>C
ENST00000483951.1:n.33T>C
NM_001139490.1:c.1492-5T>C	NP_001132962.1:n.1492-5T>C
NM_015650.3:c.1690-5T>C	NP_056465.2:n.1690-5T>C
XM_006712414.1:c.1489-5T>C	XP_006712477.1:n.1489-5T>C
XM_011510944.1:c.1792-5T>C	XP_011509246.1:n.1792-5T>C
XM_011510945.1:c.1753-5T>C	XP_011509247.1:n.1753-5T>C
XM_011510946.1:c.1720-5T>C	XP_011509248.1:n.1720-5T>C
XM_011510947.1:c.1660-5T>C	XP_011509249.1:n.1660-5T>C
XM_011510948.1:c.1594-5T>C	XP_011509250.1:n.1594-5T>C
XM_011510950.1:c.658-5T>C	XP_011509252.1:n.658-5T>C
XR_922902.1:n.1989-5T>C
XM_006712414.2:c.1489-5T>C	XP_006712477.1:n.1489-5T>C
XM_011510944.2:c.1792-5T>C	XP_011509246.1:n.1792-5T>C
XM_011510945.2:c.1753-5T>C	XP_011509247.1:n.1753-5T>C
XM_011510946.2:c.1720-5T>C	XP_011509248.1:n.1720-5T>C
XM_011510947.2:c.1660-5T>C	XP_011509249.1:n.1660-5T>C
XM_011510948.2:c.1594-5T>C	XP_011509250.1:n.1594-5T>C
XM_011510950.2:c.658-5T>C	XP_011509252.1:n.658-5T>C
XM_017003789.1:c.1789-5T>C	XP_016859278.1:n.1789-5T>C
XR_001738696.1:n.1518-5T>C
XR_001738697.1:n.1515-5T>C
XR_922902.2:n.2052-5T>C
NM_015650.4:c.1690-5T>C MANE Select	NP_056465.2:n.1690-5T>C