Canonical Allele Identifier: CA505749442

Gene: ODAD3

Linked Data

• ClinVar Variation Id: 2899322
• ClinVar RCV Id: RCV003748891
• MyVariant Identifiers: chr19:g.11533286T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422618T>C , CM000681.2:g.11422618T>C	GRCh38
NC_000019.9:g.11533286T>C , CM000681.1:g.11533286T>C	GRCh37
NC_000019.8:g.11394286T>C	NCBI36
NG_041777.1:g.18165A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1287A>G MANE Select	ENSP00000348757.3:p.Lys429=
ENST00000356392.8:c.1287A>G	ENSP00000348757.3:p.Lys429=
ENST00000586836.5:c.714A>G	ENSP00000467429.1:p.Lys238=
ENST00000591179.5:c.1107A>G	ENSP00000466800.1:p.Lys369=
ENST00000591345.5:c.*1206A>G	ENSP00000467313.1:n.*1206A>G
NM_001302453.1:c.1125A>G	NP_001289382.1:p.Lys375=
NM_001302454.1:c.1107A>G	NP_001289383.1:p.Lys369=
NM_145045.4:c.1287A>G	NP_659482.3:p.Lys429=
NM_145045.5:c.1287A>G MANE Select	NP_659482.3:p.Lys429=
NM_001302454.2:c.1107A>G	NP_001289383.1:p.Lys369=