Canonical Allele Identifier: CA2630689276

Gene: TM2D3

Linked Data

• gnomAD v4: 15-101646415-A-ACTCAGGCACTCAGGCACTAAGGCACTCAGGCACTCAGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTAAGGCACTCAGGCACTCAGGCCCTCAGGC , CM000677.2:g.101646422_101646423insACTCAGGCACTAAGGCACTCAGGCACTCAGGCCCTCAGGC	GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTAAGGCACTCAGGCACTCAGGCCCTCAGGC , CM000677.1:g.102186625_102186626insACTCAGGCACTAAGGCACTCAGGCACTCAGGCCCTCAGGC	GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTAAGGCACTCAGGCACTCAGGCCCTCAGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG MANE Select	ENSP00000330433.3:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTA...
ENST00000333202.7:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	ENSP00000330433.3:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTA...
ENST00000347970.7:c.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	ENSP00000327584.3:n.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTA...
ENST00000428002.6:c.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	ENSP00000402179.2:n.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTA...
ENST00000558129.5:c.333+309_333+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG
ENST00000558677.5:c.803+309_803+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG
ENST00000559024.5:n.832_833insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG
ENST00000559107.5:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	ENSP00000454131.1:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTA...
ENST00000559891.1:n.7_8insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG
ENST00000560013.5:c.*870+309_*870+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	ENSP00000453503.1:n.*870+309_*870+310insGGCCTGAGTGCCTGAGTGCCT...
ENST00000561373.1:c.307+309_307+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	ENSP00000452823.1:n.307+309_307+310insGGCCTGAGTGCCTGAGTGCCTTA...
NM_001307960.1:c.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_001294889.1:n.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTG...
NM_001308026.1:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_001294955.1:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTG...
NM_025141.3:c.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_079417.2:n.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCT...
NM_078474.2:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_510883.2:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCT...
NM_078474.3:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG MANE Select	NP_510883.2:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCT...
NM_001307960.2:c.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_001294889.1:n.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTG...
NM_001308026.2:c.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_001294955.1:n.502+309_502+310insGGCCTGAGTGCCTGAGTGCCTTAGTG...
NM_025141.4:c.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCTGAGTGCCTGAG	NP_079417.2:n.424+309_424+310insGGCCTGAGTGCCTGAGTGCCTTAGTGCCT...