Canonical Allele Identifier: CA301918557

Gene: TMX3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.68687909_68687912del , CM000680.2:g.68687909_68687912del	GRCh38
NC_000018.9:g.66355146_66355149del , CM000680.1:g.66355146_66355149del	GRCh37
NC_000018.8:g.64506126_64506129del	NCBI36
NG_053149.1:g.32389_32392del

Transcript Alleles

HGVS	Amino-acid Change
NM_019022.5:c.638-145_638-142del MANE Select	NP_061895.3:n.638-145_638-142del
ENST00000299608.7:c.638-145_638-142del MANE Select	ENSP00000299608.2:n.638-145_638-142del
NM_001350514.1:c.557-145_557-142del	NP_001337443.1:n.557-145_557-142del
NM_001350514.2:c.557-145_557-142del	NP_001337443.1:n.557-145_557-142del
NM_001350515.1:c.215-145_215-142del	NP_001337444.1:n.215-145_215-142del
NM_001350515.2:c.215-145_215-142del	NP_001337444.1:n.215-145_215-142del
NM_001350516.1:c.215-145_215-142del	NP_001337445.1:n.215-145_215-142del
NM_001350516.2:c.215-145_215-142del	NP_001337445.1:n.215-145_215-142del
NM_001350517.1:c.215-145_215-142del	NP_001337446.1:n.215-145_215-142del
NM_001350517.2:c.215-145_215-142del	NP_001337446.1:n.215-145_215-142del
NM_019022.3:c.638-145_638-142del	NP_061895.3:n.638-145_638-142del
NM_019022.4:c.638-145_638-142del	NP_061895.3:n.638-145_638-142del
ENST00000299608.6:c.638-145_638-142del	ENSP00000299608.2:n.638-145_638-142del
ENST00000564631.5:c.*322-145_*322-142del	ENSP00000456587.1:n.*322-145_*322-142del
ENST00000578765.1:n.68_71del
XM_005266714.1:c.215-145_215-142del	XP_005266771.1:n.215-145_215-142del
XM_011526032.1:c.764-145_764-142del	XP_011524334.1:n.764-145_764-142del
XM_011526033.1:c.215-145_215-142del	XP_011524335.1:n.215-145_215-142del
XM_011526034.3:c.*1086_*1089del	XP_011524336.1:n.*1086_*1089del
XM_011526035.3:c.*2019_*2022del	XP_011524337.1:n.*2019_*2022del
XR_935227.1:n.765-145_765-142del
XR_935227.2:n.769-145_769-142del