Canonical Allele Identifier: CA2576629764

Gene: ODAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422930_11422931del , CM000681.2:g.11422930_11422931del	GRCh38
NC_000019.9:g.11533598_11533599del , CM000681.1:g.11533598_11533599del	GRCh37
NC_000019.8:g.11394598_11394599del	NCBI36
NG_041777.1:g.17855_17856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1117-67_1117-66del MANE Select	ENSP00000348757.3:n.1117-67_1117-66del
ENST00000356392.8:c.1117-67_1117-66del	ENSP00000348757.3:n.1117-67_1117-66del
ENST00000586836.5:c.544-67_544-66del	ENSP00000467429.1:n.544-67_544-66del
ENST00000591179.5:c.937-67_937-66del	ENSP00000466800.1:n.937-67_937-66del
ENST00000591345.5:c.*1036-67_*1036-66del	ENSP00000467313.1:n.*1036-67_*1036-66del
NM_001302453.1:c.955-67_955-66del	NP_001289382.1:n.955-67_955-66del
NM_001302454.1:c.937-67_937-66del	NP_001289383.1:n.937-67_937-66del
NM_145045.4:c.1117-67_1117-66del	NP_659482.3:n.1117-67_1117-66del
XM_017026241.1:c.*11-67_*11-66del	XP_016881730.1:n.*11-67_*11-66del
NM_145045.5:c.1117-67_1117-66del MANE Select	NP_659482.3:n.1117-67_1117-66del
NM_001302454.2:c.937-67_937-66del	NP_001289383.1:n.937-67_937-66del