Canonical Allele Identifier: CA404121616

Gene: ODAD3

Linked Data

• ClinVar Variation Id: 521708
• ClinVar RCV Id: RCV000624668 ; RCV003767830
• dbSNP Id: rs1555721837
• gnomAD v4: 19-11423933-G-A
• MyVariant Identifiers: chr19:g.11534602G>A (hg19) ; chr19:g.11423933G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11423933G>A , CM000681.2:g.11423933G>A	GRCh38
NC_000019.9:g.11534602G>A , CM000681.1:g.11534602G>A	GRCh37
NC_000019.8:g.11395602G>A	NCBI36
NG_041777.1:g.16850C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1060C>T MANE Select	ENSP00000348757.3:p.Gln354Ter
ENST00000356392.8:c.1060C>T	ENSP00000348757.3:p.Gln354Ter
ENST00000586836.5:c.487C>T	ENSP00000467429.1:p.Gln163Ter
ENST00000591179.5:c.880C>T	ENSP00000466800.1:p.Gln294Ter
ENST00000591345.5:c.*979C>T	ENSP00000467313.1:n.*979C>T
NM_001302453.1:c.898C>T	NP_001289382.1:p.Gln300Ter
NM_001302454.1:c.880C>T	NP_001289383.1:p.Gln294Ter
NM_145045.4:c.1060C>T	NP_659482.3:p.Gln354Ter
XM_017026241.1:c.1001C>T	XP_016881730.1:p.Pro334Leu
NM_145045.5:c.1060C>T MANE Select	NP_659482.3:p.Gln354Ter
NM_001302454.2:c.880C>T	NP_001289383.1:p.Gln294Ter