Canonical Allele Identifier: CA9212085
Gene: ODAD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 544216
ClinVar RCV Id: RCV000655304
dbSNP Id: rs778844818

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422774G>A , CM000681.2:g.11422774G>A GRCh38
NC_000019.9:g.11533442G>A , CM000681.1:g.11533442G>A GRCh37
NC_000019.8:g.11394442G>A NCBI36
NG_041777.1:g.18009C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1204C>T MANE Select ENSP00000348757.3:p.Leu402=
ENST00000356392.8:c.1204C>T ENSP00000348757.3:p.Leu402=
ENST00000586836.5:c.631C>T ENSP00000467429.1:p.Leu211=
ENST00000591179.5:c.1024C>T ENSP00000466800.1:p.Leu342=
ENST00000591345.5:c.*1123C>T ENSP00000467313.1:n.*1123C>T
NM_001302453.1:c.1042C>T NP_001289382.1:p.Leu348=
NM_001302454.1:c.1024C>T NP_001289383.1:p.Leu342=
NM_145045.4:c.1204C>T NP_659482.3:p.Leu402=
NM_145045.5:c.1204C>T MANE Select NP_659482.3:p.Leu402=
NM_001302454.2:c.1024C>T NP_001289383.1:p.Leu342=