Canonical Allele Identifier: CA2630689180

Gene: TM2D3

Linked Data

• gnomAD v4: 15-101646409-T-TCAGGCACTCAGGCACTCAGGCACTCAGGCACTCGGGCACC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTCAGGCACTCGGGCACCCAGGCACTCAGGC , CM000677.2:g.101646422_101646423insACTCAGGCACTCAGGCACTCGGGCACCCAGGCACTCAGGC	GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTCAGGCACTCGGGCACCCAGGCACTCAGGC , CM000677.1:g.102186625_102186626insACTCAGGCACTCAGGCACTCGGGCACCCAGGCACTCAGGC	GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTCAGGCACTCGGGCACCCAGGCACTCAGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG MANE Select	ENSP00000330433.3:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCT...
ENST00000333202.7:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	ENSP00000330433.3:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCT...
ENST00000347970.7:c.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	ENSP00000327584.3:n.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCT...
ENST00000428002.6:c.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	ENSP00000402179.2:n.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCT...
ENST00000558129.5:c.333+315_333+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG
ENST00000558677.5:c.803+315_803+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG
ENST00000559024.5:n.838_839insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG
ENST00000559107.5:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	ENSP00000454131.1:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCT...
ENST00000559891.1:n.13_14insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG
ENST00000560013.5:c.*870+315_*870+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	ENSP00000453503.1:n.*870+315_*870+316insGGTGCCCGAGTGCCTGAGTGC...
ENST00000561373.1:c.307+315_307+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	ENSP00000452823.1:n.307+315_307+316insGGTGCCCGAGTGCCTGAGTGCCT...
NM_001307960.1:c.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_001294889.1:n.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAG...
NM_001308026.1:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_001294955.1:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAG...
NM_025141.3:c.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_079417.2:n.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGC...
NM_078474.2:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_510883.2:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGC...
NM_078474.3:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG MANE Select	NP_510883.2:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGC...
NM_001307960.2:c.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_001294889.1:n.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAG...
NM_001308026.2:c.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_001294955.1:n.502+315_502+316insGGTGCCCGAGTGCCTGAGTGCCTGAG...
NM_025141.4:c.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTG	NP_079417.2:n.424+315_424+316insGGTGCCCGAGTGCCTGAGTGCCTGAGTGC...