Canonical Allele Identifier: CA404120316

Gene: ODAD3

Linked Data

• gnomAD v4: 19-11422785-G-C
• MyVariant Identifiers: chr19:g.11533453G>C (hg19) ; chr19:g.11422785G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422785G>C , CM000681.2:g.11422785G>C	GRCh38
NC_000019.9:g.11533453G>C , CM000681.1:g.11533453G>C	GRCh37
NC_000019.8:g.11394453G>C	NCBI36
NG_041777.1:g.17998C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1193C>G MANE Select	ENSP00000348757.3:p.Thr398Arg
ENST00000356392.8:c.1193C>G	ENSP00000348757.3:p.Thr398Arg
ENST00000586836.5:c.620C>G	ENSP00000467429.1:p.Thr207Arg
ENST00000591179.5:c.1013C>G	ENSP00000466800.1:p.Thr338Arg
ENST00000591345.5:c.*1112C>G	ENSP00000467313.1:n.*1112C>G
NM_001302453.1:c.1031C>G	NP_001289382.1:p.Thr344Arg
NM_001302454.1:c.1013C>G	NP_001289383.1:p.Thr338Arg
NM_145045.4:c.1193C>G	NP_659482.3:p.Thr398Arg
XM_017026241.1:c.*87C>G	XP_016881730.1:n.*87C>G
NM_145045.5:c.1193C>G MANE Select	NP_659482.3:p.Thr398Arg
NM_001302454.2:c.1013C>G	NP_001289383.1:p.Thr338Arg