Canonical Allele Identifier: CA9212076

Gene: ODAD3

Linked Data

• dbSNP Id: rs759988346
• ExAC: 19:11533380 G / A
• gnomAD v2: 19-11533380-G-A
• gnomAD v4: 19-11422712-G-A
• MyVariant Identifiers: chr19:g.11533380G>A (hg19) ; chr19:g.11422712G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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