Canonical Allele Identifier: CA505749555

Gene: ODAD3

Linked Data

• MyVariant Identifiers: chr19:g.11533518C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422850C>G , CM000681.2:g.11422850C>G	GRCh38
NC_000019.9:g.11533518C>G , CM000681.1:g.11533518C>G	GRCh37
NC_000019.8:g.11394518C>G	NCBI36
NG_041777.1:g.17933G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1128G>C MANE Select	ENSP00000348757.3:p.Arg376=
ENST00000356392.8:c.1128G>C	ENSP00000348757.3:p.Arg376=
ENST00000586836.5:c.555G>C	ENSP00000467429.1:p.Arg185=
ENST00000591179.5:c.948G>C	ENSP00000466800.1:p.Arg316=
ENST00000591345.5:c.*1047G>C	ENSP00000467313.1:n.*1047G>C
NM_001302453.1:c.966G>C	NP_001289382.1:p.Arg322=
NM_001302454.1:c.948G>C	NP_001289383.1:p.Arg316=
NM_145045.4:c.1128G>C	NP_659482.3:p.Arg376=
XM_017026241.1:c.*22G>C	XP_016881730.1:n.*22G>C
NM_145045.5:c.1128G>C MANE Select	NP_659482.3:p.Arg376=
NM_001302454.2:c.948G>C	NP_001289383.1:p.Arg316=