Canonical Allele Identifier: CA505749558
Gene: ODAD3 HGNC NCBI

Linked Data

dbSNP Id: rs1395146673

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422853C>T , CM000681.2:g.11422853C>T GRCh38
NC_000019.9:g.11533521C>T , CM000681.1:g.11533521C>T GRCh37
NC_000019.8:g.11394521C>T NCBI36
NG_041777.1:g.17930G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1125G>A MANE Select ENSP00000348757.3:p.Val375=
ENST00000356392.8:c.1125G>A ENSP00000348757.3:p.Val375=
ENST00000586836.5:c.552G>A ENSP00000467429.1:p.Val184=
ENST00000591179.5:c.945G>A ENSP00000466800.1:p.Val315=
ENST00000591345.5:c.*1044G>A ENSP00000467313.1:n.*1044G>A
NM_001302453.1:c.963G>A NP_001289382.1:p.Val321=
NM_001302454.1:c.945G>A NP_001289383.1:p.Val315=
NM_145045.4:c.1125G>A NP_659482.3:p.Val375=
XM_017026241.1:c.*19G>A XP_016881730.1:n.*19G>A
NM_145045.5:c.1125G>A MANE Select NP_659482.3:p.Val375=
NM_001302454.2:c.945G>A NP_001289383.1:p.Val315=