Canonical Allele Identifier: CA505749589

Gene: ODAD3

Linked Data

• MyVariant Identifiers: chr19:g.11537051T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426231T>G , CM000681.2:g.11426231T>G	GRCh38
NC_000019.9:g.11537051T>G , CM000681.1:g.11537051T>G	GRCh37
NC_000019.8:g.11398051T>G	NCBI36
NG_041777.1:g.14552A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.876A>C MANE Select	ENSP00000348757.3:p.Arg292=
ENST00000356392.8:c.876A>C	ENSP00000348757.3:p.Arg292=
ENST00000586836.5:c.303A>C	ENSP00000467429.1:p.Arg101=
ENST00000591179.5:c.696A>C	ENSP00000466800.1:p.Arg232=
ENST00000591345.5:c.*795A>C	ENSP00000467313.1:n.*795A>C
NM_001302453.1:c.714A>C	NP_001289382.1:p.Arg238=
NM_001302454.1:c.696A>C	NP_001289383.1:p.Arg232=
NM_145045.4:c.876A>C	NP_659482.3:p.Arg292=
XM_017026241.1:c.876A>C	XP_016881730.1:p.Arg292=
NM_145045.5:c.876A>C MANE Select	NP_659482.3:p.Arg292=
NM_001302454.2:c.696A>C	NP_001289383.1:p.Arg232=