Canonical Allele Identifier: CA2630689445
Gene: TM2D3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101646425_101646426insACTCAGGCACTCAGGCGGA , CM000677.2:g.101646425_101646426insACTCAGGCACTCAGGCGGA GRCh38
NC_000015.9:g.102186628_102186629insACTCAGGCACTCAGGCGGA , CM000677.1:g.102186628_102186629insACTCAGGCACTCAGGCGGA GRCh37
NC_000015.8:g.100004151_100004152insACTCAGGCACTCAGGCGGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000333202.8:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT MANE Select ENSP00000330433.3:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
ENST00000333202.7:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT ENSP00000330433.3:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
ENST00000347970.7:c.424+299_424+300insTCCGCCTGAGTGCCTGAGT ENSP00000327584.3:n.424+299_424+300insTCCGCCTGAGTGCCTGAGT
ENST00000428002.6:c.424+299_424+300insTCCGCCTGAGTGCCTGAGT ENSP00000402179.2:n.424+299_424+300insTCCGCCTGAGTGCCTGAGT
ENST00000558129.5:c.333+299_333+300insTCCGCCTGAGTGCCTGAGT
ENST00000558677.5:c.803+299_803+300insTCCGCCTGAGTGCCTGAGT
ENST00000559024.5:n.822_823insTCCGCCTGAGTGCCTGAGT
ENST00000559107.5:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT ENSP00000454131.1:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
ENST00000560013.5:c.*870+299_*870+300insTCCGCCTGAGTGCCTGAGT ENSP00000453503.1:n.*870+299_*870+300insTCCGCCTGAGTGCCTGAGT
ENST00000561373.1:c.307+299_307+300insTCCGCCTGAGTGCCTGAGT ENSP00000452823.1:n.307+299_307+300insTCCGCCTGAGTGCCTGAGT
NM_001307960.1:c.424+299_424+300insTCCGCCTGAGTGCCTGAGT NP_001294889.1:n.424+299_424+300insTCCGCCTGAGTGCCTGAGT
NM_001308026.1:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT NP_001294955.1:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
NM_025141.3:c.424+299_424+300insTCCGCCTGAGTGCCTGAGT NP_079417.2:n.424+299_424+300insTCCGCCTGAGTGCCTGAGT
NM_078474.2:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT NP_510883.2:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
NM_078474.3:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT MANE Select NP_510883.2:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
NM_001307960.2:c.424+299_424+300insTCCGCCTGAGTGCCTGAGT NP_001294889.1:n.424+299_424+300insTCCGCCTGAGTGCCTGAGT
NM_001308026.2:c.502+299_502+300insTCCGCCTGAGTGCCTGAGT NP_001294955.1:n.502+299_502+300insTCCGCCTGAGTGCCTGAGT
NM_025141.4:c.424+299_424+300insTCCGCCTGAGTGCCTGAGT NP_079417.2:n.424+299_424+300insTCCGCCTGAGTGCCTGAGT