Canonical Allele Identifier: CA2630689238

Gene: TM2D3

Linked Data

• gnomAD v4: 15-101646413-G-GCACTCAGGCACTCAGGCACTCAGGCACTCAGGCACTCCGGCACTCAGGCACTCAGGCACTCAGGCACTCAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCCGGCACTCAGGCACTCAGGCACTCAGGCACTCAGTCACTCAGGC , CM000677.2:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCCGGCACTCAGGCACTCAGGCACTCAGGCACTCAGTCACTCAGGC	GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCCGGCACTCAGGCACTCAGGCACTCAGGCACTCAGTCACTCAGGC , CM000677.1:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCCGGCACTCAGGCACTCAGGCACTCAGGCACTCAGTCACTCAGGC	GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTCAGGCACTCAGGCACTCCGGCACTCAGGCACTCAGGCACTCAGGCACTCAGTCACTCAGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG MANE Select	ENSP00000330433.3:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000333202.7:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000330433.3:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000347970.7:c.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000327584.3:n.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000428002.6:c.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000402179.2:n.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000558129.5:c.333+311_333+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000558677.5:c.803+311_803+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000559024.5:n.834_835insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000559107.5:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000454131.1:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000559891.1:n.9_10insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000560013.5:c.*870+311_*870+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000453503.1:n.*870+311_*870+312insACTGAGTGCCTGAGTGCCTGA...
ENST00000561373.1:c.307+311_307+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000452823.1:n.307+311_307+312insACTGAGTGCCTGAGTGCCTGAGT...
NM_001307960.1:c.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294889.1:n.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_001308026.1:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294955.1:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_025141.3:c.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_079417.2:n.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_078474.2:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_510883.2:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_078474.3:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG MANE Select	NP_510883.2:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_001307960.2:c.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294889.1:n.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_001308026.2:c.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294955.1:n.502+311_502+312insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_025141.4:c.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCGGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_079417.2:n.424+311_424+312insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...