Canonical Allele Identifier: CA404126971

Gene: ODAD3

Linked Data

• ClinVar Variation Id: 477982
• ClinVar RCV Id: RCV000527261
• dbSNP Id: rs1186608353
• gnomAD v3: 19-11430777-C-G
• gnomAD v4: 19-11430777-C-G
• MyVariant Identifiers: chr19:g.11541597C>G (hg19) ; chr19:g.11430777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11430777C>G , CM000681.2:g.11430777C>G	GRCh38
NC_000019.9:g.11541597C>G , CM000681.1:g.11541597C>G	GRCh37
NC_000019.8:g.11402597C>G	NCBI36
NG_009300.1:g.329C>G
NG_041777.1:g.10006G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.367-1G>C MANE Select	ENSP00000348757.3:n.367-1G>C
ENST00000356392.8:c.367-1G>C	ENSP00000348757.3:n.367-1G>C
ENST00000586836.5:c.-207-1G>C	ENSP00000467429.1:n.-207-1G>C
ENST00000591179.5:c.366+122G>C	ENSP00000466800.1:n.366+122G>C
ENST00000591345.5:c.*286-1G>C	ENSP00000467313.1:n.*286-1G>C
ENST00000593281.1:n.250-1G>C
NM_001302453.1:c.205-1G>C	NP_001289382.1:n.205-1G>C
NM_001302454.1:c.366+122G>C	NP_001289383.1:n.366+122G>C
NM_145045.4:c.367-1G>C	NP_659482.3:n.367-1G>C
XM_017026241.1:c.367-1G>C	XP_016881730.1:n.367-1G>C
NM_145045.5:c.367-1G>C MANE Select	NP_659482.3:n.367-1G>C
NM_001302454.2:c.366+122G>C	NP_001289383.1:n.366+122G>C