Canonical Allele Identifier: CA404126681
Community Standard Title: NM_145045.5(ODAD3):c.423C>A (p.Tyr141Ter)
Gene: ODAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11430720G>T , CM000681.2:g.11430720G>T GRCh38
NC_000019.9:g.11541540G>T , CM000681.1:g.11541540G>T GRCh37
NC_000019.8:g.11402540G>T NCBI36
NG_009300.1:g.272G>T
NG_041777.1:g.10063C>A

Transcript Alleles

HGVS Amino-acid Change
NM_145045.5:c.423C>A MANE Select NP_659482.3:p.Tyr141Ter
ENST00000356392.9:c.423C>A MANE Select ENSP00000348757.3:p.Tyr141Ter
NM_001302453.1:c.261C>A NP_001289382.1:p.Tyr87Ter
NM_001302454.1:c.366+179C>A NP_001289383.1:n.366+179C>A
NM_001302454.2:c.366+179C>A NP_001289383.1:n.366+179C>A
NM_145045.4:c.423C>A NP_659482.3:p.Tyr141Ter
ENST00000356392.8:c.423C>A ENSP00000348757.3:p.Tyr141Ter
ENST00000586836.5:c.-151C>A ENSP00000467429.1:n.-151C>A
ENST00000591179.5:c.366+179C>A ENSP00000466800.1:n.366+179C>A
ENST00000591345.5:c.*342C>A ENSP00000467313.1:n.*342C>A
ENST00000593281.1:n.306C>A
XM_017026241.1:c.423C>A XP_016881730.1:p.Tyr141Ter