Canonical Allele Identifier: CA505749551
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533517G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422849G>T , CM000681.2:g.11422849G>T GRCh38
NC_000019.9:g.11533517G>T , CM000681.1:g.11533517G>T GRCh37
NC_000019.8:g.11394517G>T NCBI36
NG_041777.1:g.17934C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1129C>A MANE Select ENSP00000348757.3:p.Arg377=
ENST00000356392.8:c.1129C>A ENSP00000348757.3:p.Arg377=
ENST00000586836.5:c.556C>A ENSP00000467429.1:p.Arg186=
ENST00000591179.5:c.949C>A ENSP00000466800.1:p.Arg317=
ENST00000591345.5:c.*1048C>A ENSP00000467313.1:n.*1048C>A
NM_001302453.1:c.967C>A NP_001289382.1:p.Arg323=
NM_001302454.1:c.949C>A NP_001289383.1:p.Arg317=
NM_145045.4:c.1129C>A NP_659482.3:p.Arg377=
XM_017026241.1:c.*23C>A XP_016881730.1:n.*23C>A
NM_145045.5:c.1129C>A MANE Select NP_659482.3:p.Arg377=
NM_001302454.2:c.949C>A NP_001289383.1:p.Arg317=