Canonical Allele Identifier: CA351246365

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306234G>C (hg19) ; chr2:g.238397593G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397593G>C , CM000664.2:g.238397593G>C	GRCh38
NC_000002.11:g.239306234G>C , CM000664.1:g.239306234G>C	GRCh37
NC_000002.10:g.238970973G>C	NCBI36
NG_053055.1:g.82105G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1824G>C MANE Select	ENSP00000362424.4:p.Gln608His
ENST00000373327.4:c.1824G>C	ENSP00000362424.4:p.Gln608His
ENST00000391993.7:c.1626G>C	ENSP00000375851.3:p.Gln542His
ENST00000462122.1:n.835G>C
ENST00000483951.1:n.172G>C
NM_001139490.1:c.1626G>C	NP_001132962.1:p.Gln542His
NM_015650.3:c.1824G>C	NP_056465.2:p.Gln608His
XM_006712414.1:c.1623G>C	XP_006712477.1:p.Gln541His
XM_011510944.1:c.1926G>C	XP_011509246.1:p.Gln642His
XM_011510945.1:c.1887G>C	XP_011509247.1:p.Gln629His
XM_011510946.1:c.1854G>C	XP_011509248.1:p.Gln618His
XM_011510947.1:c.1794G>C	XP_011509249.1:p.Gln598His
XM_011510948.1:c.1728G>C	XP_011509250.1:p.Gln576His
XM_011510950.1:c.792G>C	XP_011509252.1:p.Gln264His
XM_006712414.2:c.1623G>C	XP_006712477.1:p.Gln541His
XM_011510944.2:c.1926G>C	XP_011509246.1:p.Gln642His
XM_011510945.2:c.1887G>C	XP_011509247.1:p.Gln629His
XM_011510946.2:c.1854G>C	XP_011509248.1:p.Gln618His
XM_011510947.2:c.1794G>C	XP_011509249.1:p.Gln598His
XM_011510948.2:c.1728G>C	XP_011509250.1:p.Gln576His
XM_011510950.2:c.792G>C	XP_011509252.1:p.Gln264His
XM_017003789.1:c.1923G>C	XP_016859278.1:p.Gln641His
XR_001738696.1:n.1652G>C
XR_001738697.1:n.1649G>C
NM_015650.4:c.1824G>C MANE Select	NP_056465.2:p.Gln608His