Canonical Allele Identifier: CA404120509

Gene: ODAD3

Linked Data

• dbSNP Id: rs1381391963
• gnomAD v2: 19-11533501-C-T
• gnomAD v4: 19-11422833-C-T
• MyVariant Identifiers: chr19:g.11533501C>T (hg19) ; chr19:g.11422833C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422833C>T , CM000681.2:g.11422833C>T	GRCh38
NC_000019.9:g.11533501C>T , CM000681.1:g.11533501C>T	GRCh37
NC_000019.8:g.11394501C>T	NCBI36
NG_041777.1:g.17950G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1145G>A MANE Select	ENSP00000348757.3:p.Gly382Asp
ENST00000356392.8:c.1145G>A	ENSP00000348757.3:p.Gly382Asp
ENST00000586836.5:c.572G>A	ENSP00000467429.1:p.Gly191Asp
ENST00000591179.5:c.965G>A	ENSP00000466800.1:p.Gly322Asp
ENST00000591345.5:c.*1064G>A	ENSP00000467313.1:n.*1064G>A
NM_001302453.1:c.983G>A	NP_001289382.1:p.Gly328Asp
NM_001302454.1:c.965G>A	NP_001289383.1:p.Gly322Asp
NM_145045.4:c.1145G>A	NP_659482.3:p.Gly382Asp
XM_017026241.1:c.*39G>A	XP_016881730.1:n.*39G>A
NM_145045.5:c.1145G>A MANE Select	NP_659482.3:p.Gly382Asp
NM_001302454.2:c.965G>A	NP_001289383.1:p.Gly322Asp