Canonical Allele Identifier: CA505749456
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533380G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422712G>C , CM000681.2:g.11422712G>C GRCh38
NC_000019.9:g.11533380G>C , CM000681.1:g.11533380G>C GRCh37
NC_000019.8:g.11394380G>C NCBI36
NG_041777.1:g.18071C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1266C>G MANE Select ENSP00000348757.3:p.Ala422=
ENST00000356392.8:c.1266C>G ENSP00000348757.3:p.Ala422=
ENST00000586836.5:c.693C>G ENSP00000467429.1:p.Ala231=
ENST00000591179.5:c.1086C>G ENSP00000466800.1:p.Ala362=
ENST00000591345.5:c.*1185C>G ENSP00000467313.1:n.*1185C>G
NM_001302453.1:c.1104C>G NP_001289382.1:p.Ala368=
NM_001302454.1:c.1086C>G NP_001289383.1:p.Ala362=
NM_145045.4:c.1266C>G NP_659482.3:p.Ala422=
NM_145045.5:c.1266C>G MANE Select NP_659482.3:p.Ala422=
NM_001302454.2:c.1086C>G NP_001289383.1:p.Ala362=