Canonical Allele Identifier: CA2630689359

Gene: TM2D3

Linked Data

• gnomAD v4: 15-101646421-G-GCACTCAGGCACTCAGGCACTCAGGCACTCAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCAGTC , CM000677.2:g.101646422_101646423insACTCAGGCACTCAGGCACTCAGGCACTCAGTC	GRCh38
NC_000015.9:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCAGTC , CM000677.1:g.102186625_102186626insACTCAGGCACTCAGGCACTCAGGCACTCAGTC	GRCh37
NC_000015.8:g.100004148_100004149insACTCAGGCACTCAGGCACTCAGGCACTCAGTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG MANE Select	ENSP00000330433.3:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000333202.7:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000330433.3:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000347970.7:c.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000327584.3:n.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000428002.6:c.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000402179.2:n.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000558129.5:c.333+303_333+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000558677.5:c.803+303_803+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000559024.5:n.826_827insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000559107.5:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000454131.1:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGT...
ENST00000559891.1:n.1_2insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG
ENST00000560013.5:c.*870+303_*870+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000453503.1:n.*870+303_*870+304insACTGAGTGCCTGAGTGCCTGA...
ENST00000561373.1:c.307+303_307+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	ENSP00000452823.1:n.307+303_307+304insACTGAGTGCCTGAGTGCCTGAGT...
NM_001307960.1:c.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294889.1:n.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_001308026.1:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294955.1:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_025141.3:c.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_079417.2:n.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_078474.2:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_510883.2:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_078474.3:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG MANE Select	NP_510883.2:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...
NM_001307960.2:c.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294889.1:n.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_001308026.2:c.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_001294955.1:n.502+303_502+304insACTGAGTGCCTGAGTGCCTGAGTGCC...
NM_025141.4:c.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGAGTG	NP_079417.2:n.424+303_424+304insACTGAGTGCCTGAGTGCCTGAGTGCCTGA...