Canonical Allele Identifier: CA404122913

Gene: ODAD3

Linked Data

• dbSNP Id: rs587777779
• gnomAD v4: 19-11426182-C-G
• MyVariant Identifiers: chr19:g.11537002C>G (hg19) ; chr19:g.11426182C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426182C>G , CM000681.2:g.11426182C>G	GRCh38
NC_000019.9:g.11537002C>G , CM000681.1:g.11537002C>G	GRCh37
NC_000019.8:g.11398002C>G	NCBI36
NG_041777.1:g.14601G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356392.9:c.925G>C MANE Select	ENSP00000348757.3:p.Glu309Gln
ENST00000356392.8:c.925G>C	ENSP00000348757.3:p.Glu309Gln
ENST00000586836.5:c.352G>C	ENSP00000467429.1:p.Glu118Gln
ENST00000591179.5:c.745G>C	ENSP00000466800.1:p.Glu249Gln
ENST00000591345.5:c.*844G>C	ENSP00000467313.1:n.*844G>C
NM_001302453.1:c.763G>C	NP_001289382.1:p.Glu255Gln
NM_001302454.1:c.745G>C	NP_001289383.1:p.Glu249Gln
NM_145045.4:c.925G>C	NP_659482.3:p.Glu309Gln
XM_017026241.1:c.904+21G>C	XP_016881730.1:n.904+21G>C
NM_145045.5:c.925G>C MANE Select	NP_659482.3:p.Glu309Gln
NM_001302454.2:c.745G>C	NP_001289383.1:p.Glu249Gln