Canonical Allele Identifier: CA2805490103

Gene: TM2D3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTAAGGCACTCAGGC , CM000677.2:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTAAGGCACTCAGGC	GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTAAGGCACTCAGGC , CM000677.1:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTAAGGCACTCAGGC	GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTAAGGCACTCAGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT MANE Select	ENSP00000330433.3:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCC...
ENST00000333202.7:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	ENSP00000330433.3:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCC...
ENST00000347970.7:c.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	ENSP00000327584.3:n.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCC...
ENST00000428002.6:c.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	ENSP00000402179.2:n.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCC...
ENST00000558129.5:c.333+314_333+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT
ENST00000558677.5:c.803+314_803+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT
ENST00000559024.5:n.837_838insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT
ENST00000559107.5:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	ENSP00000454131.1:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCC...
ENST00000559891.1:n.12_13insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT
ENST00000560013.5:c.*870+314_*870+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	ENSP00000453503.1:n.*870+314_*870+315insTAGTGCCTGAGTGCCTGAGTG...
ENST00000561373.1:c.307+314_307+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	ENSP00000452823.1:n.307+314_307+315insTAGTGCCTGAGTGCCTGAGTGCC...
NM_001307960.1:c.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_001294889.1:n.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_001308026.1:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_001294955.1:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_025141.3:c.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_079417.2:n.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_078474.2:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_510883.2:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_078474.3:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT MANE Select	NP_510883.2:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_001307960.2:c.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_001294889.1:n.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_001308026.2:c.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_001294955.1:n.502+314_502+315insTAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_025141.4:c.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCT	NP_079417.2:n.424+314_424+315insTAGTGCCTGAGTGCCTGAGTGCCTGAGTG...