Canonical Allele Identifier: CA2630689155
Gene: TM2D3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCAGGCTCTCAGGCACTCAGGC , CM000677.2:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCAGGCTCTCAGGCACTCAGGC GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCAGGCTCTCAGGCACTCAGGC , CM000677.1:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCAGGCTCTCAGGCACTCAGGC GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTCAGGCACTCAGGCACTCAGGCTCTCAGGCACTCAGGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000333202.8:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG MANE Select ENSP00000330433.3:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGA...
ENST00000333202.7:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG ENSP00000330433.3:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGA...
ENST00000347970.7:c.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG ENSP00000327584.3:n.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGA...
ENST00000428002.6:c.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG ENSP00000402179.2:n.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGA...
ENST00000558129.5:c.333+317_333+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000558677.5:c.803+317_803+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000559024.5:n.840_841insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000559107.5:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG ENSP00000454131.1:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGA...
ENST00000559891.1:n.15_16insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG
ENST00000560013.5:c.*870+317_*870+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG ENSP00000453503.1:n.*870+317_*870+318insAGCCTGAGTGCCTGAGTGCCT...
ENST00000561373.1:c.307+317_307+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG ENSP00000452823.1:n.307+317_307+318insAGCCTGAGTGCCTGAGTGCCTGA...
NM_001307960.1:c.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_001294889.1:n.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_001308026.1:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_001294955.1:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_025141.3:c.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_079417.2:n.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCT...
NM_078474.2:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_510883.2:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCT...
NM_078474.3:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG MANE Select NP_510883.2:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCT...
NM_001307960.2:c.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_001294889.1:n.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_001308026.2:c.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_001294955.1:n.502+317_502+318insAGCCTGAGTGCCTGAGTGCCTGAGTG...
NM_025141.4:c.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAGTGCCTGAG NP_079417.2:n.424+317_424+318insAGCCTGAGTGCCTGAGTGCCTGAGTGCCT...