Canonical Allele Identifier: CA404119906

Gene: ODAD3

Linked Data

• gnomAD v4: 19-11422610-G-T
• MyVariant Identifiers: chr19:g.11533278G>T (hg19) ; chr19:g.11422610G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422610G>T , CM000681.2:g.11422610G>T	GRCh38
NC_000019.9:g.11533278G>T , CM000681.1:g.11533278G>T	GRCh37
NC_000019.8:g.11394278G>T	NCBI36
NG_041777.1:g.18173C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1295C>A MANE Select	ENSP00000348757.3:p.Ala432Asp
ENST00000356392.8:c.1295C>A	ENSP00000348757.3:p.Ala432Asp
ENST00000586836.5:c.722C>A	ENSP00000467429.1:p.Ala241Asp
ENST00000591179.5:c.1115C>A	ENSP00000466800.1:p.Ala372Asp
ENST00000591345.5:c.*1214C>A	ENSP00000467313.1:n.*1214C>A
NM_001302453.1:c.1133C>A	NP_001289382.1:p.Ala378Asp
NM_001302454.1:c.1115C>A	NP_001289383.1:p.Ala372Asp
NM_145045.4:c.1295C>A	NP_659482.3:p.Ala432Asp
NM_145045.5:c.1295C>A MANE Select	NP_659482.3:p.Ala432Asp
NM_001302454.2:c.1115C>A	NP_001289383.1:p.Ala372Asp