Canonical Allele Identifier: CA432228238

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306210G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397569G>C , CM000664.2:g.238397569G>C	GRCh38
NC_000002.11:g.239306210G>C , CM000664.1:g.239306210G>C	GRCh37
NC_000002.10:g.238970949G>C	NCBI36
NG_053055.1:g.82081G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1800G>C MANE Select	ENSP00000362424.4:p.Leu600=
ENST00000373327.4:c.1800G>C	ENSP00000362424.4:p.Leu600=
ENST00000391993.7:c.1602G>C	ENSP00000375851.3:p.Leu534=
ENST00000462122.1:n.811G>C
ENST00000483951.1:n.148G>C
NM_001139490.1:c.1602G>C	NP_001132962.1:p.Leu534=
NM_015650.3:c.1800G>C	NP_056465.2:p.Leu600=
XM_006712414.1:c.1599G>C	XP_006712477.1:p.Leu533=
XM_011510944.1:c.1902G>C	XP_011509246.1:p.Leu634=
XM_011510945.1:c.1863G>C	XP_011509247.1:p.Leu621=
XM_011510946.1:c.1830G>C	XP_011509248.1:p.Leu610=
XM_011510947.1:c.1770G>C	XP_011509249.1:p.Leu590=
XM_011510948.1:c.1704G>C	XP_011509250.1:p.Leu568=
XM_011510950.1:c.768G>C	XP_011509252.1:p.Leu256=
XM_006712414.2:c.1599G>C	XP_006712477.1:p.Leu533=
XM_011510944.2:c.1902G>C	XP_011509246.1:p.Leu634=
XM_011510945.2:c.1863G>C	XP_011509247.1:p.Leu621=
XM_011510946.2:c.1830G>C	XP_011509248.1:p.Leu610=
XM_011510947.2:c.1770G>C	XP_011509249.1:p.Leu590=
XM_011510948.2:c.1704G>C	XP_011509250.1:p.Leu568=
XM_011510950.2:c.768G>C	XP_011509252.1:p.Leu256=
XM_017003789.1:c.1899G>C	XP_016859278.1:p.Leu633=
XR_001738696.1:n.1628G>C
XR_001738697.1:n.1625G>C
NM_015650.4:c.1800G>C MANE Select	NP_056465.2:p.Leu600=