Canonical Allele Identifier: CA404120315

Gene: ODAD3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1193C>T MANE Select	ENSP00000348757.3:p.Thr398Met
ENST00000356392.8:c.1193C>T	ENSP00000348757.3:p.Thr398Met
ENST00000586836.5:c.620C>T	ENSP00000467429.1:p.Thr207Met
ENST00000591179.5:c.1013C>T	ENSP00000466800.1:p.Thr338Met
ENST00000591345.5:c.*1112C>T	ENSP00000467313.1:n.*1112C>T
NM_001302453.1:c.1031C>T	NP_001289382.1:p.Thr344Met
NM_001302454.1:c.1013C>T	NP_001289383.1:p.Thr338Met
NM_145045.4:c.1193C>T	NP_659482.3:p.Thr398Met
XM_017026241.1:c.*87C>T	XP_016881730.1:n.*87C>T
NM_145045.5:c.1193C>T MANE Select	NP_659482.3:p.Thr398Met
NM_001302454.2:c.1013C>T	NP_001289383.1:p.Thr338Met