Canonical Allele Identifier: CA404119333

Gene: ODAD3

Linked Data

• ClinVar Variation Id: 544215
• ClinVar RCV Id: RCV000655303
• dbSNP Id: rs1340885760
• MyVariant Identifiers: chr19:g.11532445G>C (hg19) ; chr19:g.11421777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11421777G>C , CM000681.2:g.11421777G>C	GRCh38
NC_000019.9:g.11532445G>C , CM000681.1:g.11532445G>C	GRCh37
NC_000019.8:g.11393445G>C	NCBI36
NG_041777.1:g.19006C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1490C>G MANE Select	ENSP00000348757.3:p.Pro497Arg
ENST00000356392.8:c.1490C>G	ENSP00000348757.3:p.Pro497Arg
ENST00000586836.5:c.917C>G	ENSP00000467429.1:p.Pro306Arg
ENST00000591179.5:c.1310C>G	ENSP00000466800.1:p.Pro437Arg
ENST00000591345.5:c.*1409C>G	ENSP00000467313.1:n.*1409C>G
NM_001302453.1:c.1328C>G	NP_001289382.1:p.Pro443Arg
NM_001302454.1:c.1310C>G	NP_001289383.1:p.Pro437Arg
NM_145045.4:c.1490C>G	NP_659482.3:p.Pro497Arg
NM_145045.5:c.1490C>G MANE Select	NP_659482.3:p.Pro497Arg
NM_001302454.2:c.1310C>G	NP_001289383.1:p.Pro437Arg