Canonical Allele Identifier: CA351246607

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306270G>C (hg19) ; chr2:g.238397629G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397629G>C , CM000664.2:g.238397629G>C	GRCh38
NC_000002.11:g.239306270G>C , CM000664.1:g.239306270G>C	GRCh37
NC_000002.10:g.238971009G>C	NCBI36
NG_053055.1:g.82141G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373327.5:c.1860G>C MANE Select	ENSP00000362424.4:p.Met620Ile
ENST00000373327.4:c.1860G>C	ENSP00000362424.4:p.Met620Ile
ENST00000391993.7:c.1662G>C	ENSP00000375851.3:p.Met554Ile
ENST00000462122.1:n.871G>C
ENST00000483951.1:n.208G>C
NM_001139490.1:c.1662G>C	NP_001132962.1:p.Met554Ile
NM_015650.3:c.1860G>C	NP_056465.2:p.Met620Ile
XM_006712414.1:c.1659G>C	XP_006712477.1:p.Met553Ile
XM_011510944.1:c.1962G>C	XP_011509246.1:p.Met654Ile
XM_011510945.1:c.1923G>C	XP_011509247.1:p.Met641Ile
XM_011510946.1:c.1890G>C	XP_011509248.1:p.Met630Ile
XM_011510947.1:c.1830G>C	XP_011509249.1:p.Met610Ile
XM_011510948.1:c.1764G>C	XP_011509250.1:p.Met588Ile
XM_011510950.1:c.828G>C	XP_011509252.1:p.Met276Ile
XM_006712414.2:c.1659G>C	XP_006712477.1:p.Met553Ile
XM_011510944.2:c.1962G>C	XP_011509246.1:p.Met654Ile
XM_011510945.2:c.1923G>C	XP_011509247.1:p.Met641Ile
XM_011510946.2:c.1890G>C	XP_011509248.1:p.Met630Ile
XM_011510947.2:c.1830G>C	XP_011509249.1:p.Met610Ile
XM_011510948.2:c.1764G>C	XP_011509250.1:p.Met588Ile
XM_011510950.2:c.828G>C	XP_011509252.1:p.Met276Ile
XM_017003789.1:c.1959G>C	XP_016859278.1:p.Met653Ile
XR_001738696.1:n.1688G>C
XR_001738697.1:n.1685G>C
NM_015650.4:c.1860G>C MANE Select	NP_056465.2:p.Met620Ile