Canonical Allele Identifier: CA783271440

Gene: ODAD3

Linked Data

• dbSNP Id: rs1290823280
• MyVariant Identifiers: chr19:g.11533361T>A (hg19) ; chr19:g.11422693T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422693T>A , CM000681.2:g.11422693T>A	GRCh38
NC_000019.9:g.11533361T>A , CM000681.1:g.11533361T>A	GRCh37
NC_000019.8:g.11394361T>A	NCBI36
NG_041777.1:g.18090A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1277+8A>T MANE Select	ENSP00000348757.3:n.1277+8A>T
ENST00000356392.8:c.1277+8A>T	ENSP00000348757.3:n.1277+8A>T
ENST00000586836.5:c.704+8A>T	ENSP00000467429.1:n.704+8A>T
ENST00000591179.5:c.1097+8A>T	ENSP00000466800.1:n.1097+8A>T
ENST00000591345.5:c.*1196+8A>T	ENSP00000467313.1:n.*1196+8A>T
NM_001302453.1:c.1115+8A>T	NP_001289382.1:n.1115+8A>T
NM_001302454.1:c.1097+8A>T	NP_001289383.1:n.1097+8A>T
NM_145045.4:c.1277+8A>T	NP_659482.3:n.1277+8A>T
NM_145045.5:c.1277+8A>T MANE Select	NP_659482.3:n.1277+8A>T
NM_001302454.2:c.1097+8A>T	NP_001289383.1:n.1097+8A>T