Canonical Allele Identifier: CA505749561
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533526A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422858A>G , CM000681.2:g.11422858A>G GRCh38
NC_000019.9:g.11533526A>G , CM000681.1:g.11533526A>G GRCh37
NC_000019.8:g.11394526A>G NCBI36
NG_041777.1:g.17925T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1120T>C MANE Select ENSP00000348757.3:p.Leu374=
ENST00000356392.8:c.1120T>C ENSP00000348757.3:p.Leu374=
ENST00000586836.5:c.547T>C ENSP00000467429.1:p.Leu183=
ENST00000591179.5:c.940T>C ENSP00000466800.1:p.Leu314=
ENST00000591345.5:c.*1039T>C ENSP00000467313.1:n.*1039T>C
NM_001302453.1:c.958T>C NP_001289382.1:p.Leu320=
NM_001302454.1:c.940T>C NP_001289383.1:p.Leu314=
NM_145045.4:c.1120T>C NP_659482.3:p.Leu374=
XM_017026241.1:c.*14T>C XP_016881730.1:n.*14T>C
NM_145045.5:c.1120T>C MANE Select NP_659482.3:p.Leu374=
NM_001302454.2:c.940T>C NP_001289383.1:p.Leu314=