Canonical Allele Identifier: CA505749529

Gene: ODAD3

Linked Data

• MyVariant Identifiers: chr19:g.11533500G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422832G>C , CM000681.2:g.11422832G>C	GRCh38
NC_000019.9:g.11533500G>C , CM000681.1:g.11533500G>C	GRCh37
NC_000019.8:g.11394500G>C	NCBI36
NG_041777.1:g.17951C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1146C>G MANE Select	ENSP00000348757.3:p.Gly382=
ENST00000356392.8:c.1146C>G	ENSP00000348757.3:p.Gly382=
ENST00000586836.5:c.573C>G	ENSP00000467429.1:p.Gly191=
ENST00000591179.5:c.966C>G	ENSP00000466800.1:p.Gly322=
ENST00000591345.5:c.*1065C>G	ENSP00000467313.1:n.*1065C>G
NM_001302453.1:c.984C>G	NP_001289382.1:p.Gly328=
NM_001302454.1:c.966C>G	NP_001289383.1:p.Gly322=
NM_145045.4:c.1146C>G	NP_659482.3:p.Gly382=
XM_017026241.1:c.*40C>G	XP_016881730.1:n.*40C>G
NM_145045.5:c.1146C>G MANE Select	NP_659482.3:p.Gly382=
NM_001302454.2:c.966C>G	NP_001289383.1:p.Gly322=