Canonical Allele Identifier: CA9212087

Gene: ODAD3

Linked Data

• dbSNP Id: rs758184941
• ExAC: 19:11533452 C / G
• gnomAD v2: 19-11533452-C-G
• gnomAD v3: 19-11422784-C-G
• gnomAD v4: 19-11422784-C-G
• MyVariant Identifiers: chr19:g.11533452C>G (hg19) ; chr19:g.11422784C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422784C>G , CM000681.2:g.11422784C>G	GRCh38
NC_000019.9:g.11533452C>G , CM000681.1:g.11533452C>G	GRCh37
NC_000019.8:g.11394452C>G	NCBI36
NG_041777.1:g.17999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1194G>C MANE Select	ENSP00000348757.3:p.Thr398=
ENST00000356392.8:c.1194G>C	ENSP00000348757.3:p.Thr398=
ENST00000586836.5:c.621G>C	ENSP00000467429.1:p.Thr207=
ENST00000591179.5:c.1014G>C	ENSP00000466800.1:p.Thr338=
ENST00000591345.5:c.*1113G>C	ENSP00000467313.1:n.*1113G>C
NM_001302453.1:c.1032G>C	NP_001289382.1:p.Thr344=
NM_001302454.1:c.1014G>C	NP_001289383.1:p.Thr338=
NM_145045.4:c.1194G>C	NP_659482.3:p.Thr398=
XM_017026241.1:c.*88G>C	XP_016881730.1:n.*88G>C
NM_145045.5:c.1194G>C MANE Select	NP_659482.3:p.Thr398=
NM_001302454.2:c.1014G>C	NP_001289383.1:p.Thr338=