Canonical Allele Identifier: CA505749429
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533268C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422600C>T , CM000681.2:g.11422600C>T GRCh38
NC_000019.9:g.11533268C>T , CM000681.1:g.11533268C>T GRCh37
NC_000019.8:g.11394268C>T NCBI36
NG_041777.1:g.18183G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1305G>A MANE Select ENSP00000348757.3:p.Gln435=
ENST00000356392.8:c.1305G>A ENSP00000348757.3:p.Gln435=
ENST00000586836.5:c.732G>A ENSP00000467429.1:p.Gln244=
ENST00000591179.5:c.1125G>A ENSP00000466800.1:p.Gln375=
ENST00000591345.5:c.*1224G>A ENSP00000467313.1:n.*1224G>A
NM_001302453.1:c.1143G>A NP_001289382.1:p.Gln381=
NM_001302454.1:c.1125G>A NP_001289383.1:p.Gln375=
NM_145045.4:c.1305G>A NP_659482.3:p.Gln435=
NM_145045.5:c.1305G>A MANE Select NP_659482.3:p.Gln435=
NM_001302454.2:c.1125G>A NP_001289383.1:p.Gln375=