Canonical Allele Identifier: CA2805490114

Gene: TM2D3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTCAGGCAGTCAGGCACTCAGGCACTCAGGCGCTCAGGC , CM000677.2:g.101646422_101646423insACTCAGGCACTCAGGCAGTCAGGCACTCAGGCACTCAGGCGCTCAGGC	GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTCAGGCAGTCAGGCACTCAGGCACTCAGGCGCTCAGGC , CM000677.1:g.102186625_102186626insACTCAGGCACTCAGGCAGTCAGGCACTCAGGCACTCAGGCGCTCAGGC	GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTCAGGCAGTCAGGCACTCAGGCACTCAGGCGCTCAGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG MANE Select	ENSP00000330433.3:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGA...
ENST00000333202.7:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	ENSP00000330433.3:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGA...
ENST00000347970.7:c.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	ENSP00000327584.3:n.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGA...
ENST00000428002.6:c.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	ENSP00000402179.2:n.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGA...
ENST00000558129.5:c.333+309_333+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000558677.5:c.803+309_803+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000559024.5:n.832_833insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000559107.5:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	ENSP00000454131.1:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGA...
ENST00000559891.1:n.7_8insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000560013.5:c.*870+309_*870+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	ENSP00000453503.1:n.*870+309_*870+310insCGCCTGAGTGCCTGAGTGCCT...
ENST00000561373.1:c.307+309_307+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	ENSP00000452823.1:n.307+309_307+310insCGCCTGAGTGCCTGAGTGCCTGA...
NM_001307960.1:c.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_001294889.1:n.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTG...
NM_001308026.1:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_001294955.1:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTG...
NM_025141.3:c.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_079417.2:n.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCT...
NM_078474.2:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_510883.2:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCT...
NM_078474.3:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG MANE Select	NP_510883.2:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCT...
NM_001307960.2:c.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_001294889.1:n.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTG...
NM_001308026.2:c.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_001294955.1:n.502+309_502+310insCGCCTGAGTGCCTGAGTGCCTGACTG...
NM_025141.4:c.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCTGAGTGCCTGAGTGCCTGAG	NP_079417.2:n.424+309_424+310insCGCCTGAGTGCCTGAGTGCCTGACTGCCT...