Canonical Allele Identifier: CA505749568
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11537009C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11426189C>T , CM000681.2:g.11426189C>T GRCh38
NC_000019.9:g.11537009C>T , CM000681.1:g.11537009C>T GRCh37
NC_000019.8:g.11398009C>T NCBI36
NG_041777.1:g.14594G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356392.9:c.918G>A MANE Select ENSP00000348757.3:p.Lys306=
ENST00000356392.8:c.918G>A ENSP00000348757.3:p.Lys306=
ENST00000586836.5:c.345G>A ENSP00000467429.1:p.Lys115=
ENST00000591179.5:c.738G>A ENSP00000466800.1:p.Lys246=
ENST00000591345.5:c.*837G>A ENSP00000467313.1:n.*837G>A
NM_001302453.1:c.756G>A NP_001289382.1:p.Lys252=
NM_001302454.1:c.738G>A NP_001289383.1:p.Lys246=
NM_145045.4:c.918G>A NP_659482.3:p.Lys306=
XM_017026241.1:c.904+14G>A XP_016881730.1:n.904+14G>A
NM_145045.5:c.918G>A MANE Select NP_659482.3:p.Lys306=
NM_001302454.2:c.738G>A NP_001289383.1:p.Lys246=