Canonical Allele Identifier: CA2630689296

Gene: TM2D3

Linked Data

• gnomAD v4: 15-101646416-C-CTCAGCCACTCAGGCACTCAGGCACTCAGGCACTCAGGCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646420_101646421insCCACTCAGGCACTCAGGCACTCAGGCACTCAGGCATTCAG , CM000677.2:g.101646420_101646421insCCACTCAGGCACTCAGGCACTCAGGCACTCAGGCATTCAG	GRCh38
NC_000015.9:g.102186623_102186624insCCACTCAGGCACTCAGGCACTCAGGCACTCAGGCATTCAG , CM000677.1:g.102186623_102186624insCCACTCAGGCACTCAGGCACTCAGGCACTCAGGCATTCAG	GRCh37
NC_000015.8:g.100004146_100004147insCCACTCAGGCACTCAGGCACTCAGGCACTCAGGCATTCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA MANE Select	ENSP00000330433.3:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTG...
ENST00000333202.7:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	ENSP00000330433.3:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTG...
ENST00000347970.7:c.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	ENSP00000327584.3:n.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTG...
ENST00000428002.6:c.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	ENSP00000402179.2:n.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTG...
ENST00000558129.5:c.333+308_333+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA
ENST00000558677.5:c.803+308_803+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA
ENST00000559024.5:n.831_832insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA
ENST00000559107.5:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	ENSP00000454131.1:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTG...
ENST00000559891.1:n.6_7insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA
ENST00000560013.5:c.*870+308_*870+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	ENSP00000453503.1:n.*870+308_*870+309insATGCCTGAGTGCCTGAGTGCC...
ENST00000561373.1:c.307+308_307+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	ENSP00000452823.1:n.307+308_307+309insATGCCTGAGTGCCTGAGTGCCTG...
NM_001307960.1:c.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_001294889.1:n.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGT...
NM_001308026.1:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_001294955.1:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGT...
NM_025141.3:c.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_079417.2:n.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCC...
NM_078474.2:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_510883.2:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCC...
NM_078474.3:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA MANE Select	NP_510883.2:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCC...
NM_001307960.2:c.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_001294889.1:n.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGT...
NM_001308026.2:c.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_001294955.1:n.502+308_502+309insATGCCTGAGTGCCTGAGTGCCTGAGT...
NM_025141.4:c.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGGCTGA	NP_079417.2:n.424+308_424+309insATGCCTGAGTGCCTGAGTGCCTGAGTGCC...