Canonical Allele Identifier: CA2322925139

Gene: ODAD3

Linked Data

• dbSNP Id: rs1969178450
• gnomAD v4: 19-11423003-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11423006_11423007del , CM000681.2:g.11423006_11423007del	GRCh38
NC_000019.9:g.11533674_11533675del , CM000681.1:g.11533674_11533675del	GRCh37
NC_000019.8:g.11394674_11394675del	NCBI36
NG_041777.1:g.17778_17779del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1117-144_1117-143del MANE Select	ENSP00000348757.3:n.1117-144_1117-143del
ENST00000356392.8:c.1117-144_1117-143del	ENSP00000348757.3:n.1117-144_1117-143del
ENST00000586836.5:c.544-144_544-143del	ENSP00000467429.1:n.544-144_544-143del
ENST00000591179.5:c.937-144_937-143del	ENSP00000466800.1:n.937-144_937-143del
ENST00000591345.5:c.*1036-144_*1036-143del	ENSP00000467313.1:n.*1036-144_*1036-143del
NM_001302453.1:c.955-144_955-143del	NP_001289382.1:n.955-144_955-143del
NM_001302454.1:c.937-144_937-143del	NP_001289383.1:n.937-144_937-143del
NM_145045.4:c.1117-144_1117-143del	NP_659482.3:n.1117-144_1117-143del
XM_017026241.1:c.*11-144_*11-143del	XP_016881730.1:n.*11-144_*11-143del
NM_145045.5:c.1117-144_1117-143del MANE Select	NP_659482.3:n.1117-144_1117-143del
NM_001302454.2:c.937-144_937-143del	NP_001289383.1:n.937-144_937-143del