Canonical Allele Identifier: CA505749411
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533241C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422573C>G , CM000681.2:g.11422573C>G GRCh38
NC_000019.9:g.11533241C>G , CM000681.1:g.11533241C>G GRCh37
NC_000019.8:g.11394241C>G NCBI36
NG_041777.1:g.18210G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1332G>C MANE Select ENSP00000348757.3:p.Arg444=
ENST00000356392.8:c.1332G>C ENSP00000348757.3:p.Arg444=
ENST00000586836.5:c.759G>C ENSP00000467429.1:p.Arg253=
ENST00000591179.5:c.1152G>C ENSP00000466800.1:p.Arg384=
ENST00000591345.5:c.*1251G>C ENSP00000467313.1:n.*1251G>C
NM_001302453.1:c.1170G>C NP_001289382.1:p.Arg390=
NM_001302454.1:c.1152G>C NP_001289383.1:p.Arg384=
NM_145045.4:c.1332G>C NP_659482.3:p.Arg444=
NM_145045.5:c.1332G>C MANE Select NP_659482.3:p.Arg444=
NM_001302454.2:c.1152G>C NP_001289383.1:p.Arg384=