Canonical Allele Identifier: CA2637885023
Community Standard Title: NM_031421.5(ODAD4):c.398-66A>G
Gene: ODAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41936407A>G , CM000679.2:g.41936407A>G GRCh38
NC_000017.10:g.40092660A>G , CM000679.1:g.40092660A>G GRCh37
NC_000017.9:g.37346186A>G NCBI36
NG_053115.1:g.10814A>G

Transcript Alleles

HGVS Amino-acid Change
NM_031421.5:c.398-66A>G MANE Select NP_113609.1:n.398-66A>G
ENST00000377540.6:c.398-66A>G MANE Select ENSP00000478589.1:n.398-66A>G
NM_001350319.1:c.398-66A>G NP_001337248.1:n.398-66A>G
NM_001350319.2:c.398-66A>G NP_001337248.1:n.398-66A>G
NM_031421.3:c.398-66A>G NP_113609.1:n.398-66A>G
NM_031421.4:c.398-66A>G NP_113609.1:n.398-66A>G
NR_110662.1:n.499-66A>G
NR_110662.2:n.528-66A>G
NR_110662.3:n.505-66A>G
NR_146621.1:n.450-66A>G
NR_146621.2:n.427-66A>G
NR_146622.1:n.450-66A>G
NR_146622.2:n.427-66A>G
ENST00000377540.5:c.398-66A>G ENSP00000478589.1:n.398-66A>G
ENST00000585530.1:c.125-66A>G ENSP00000479460.1:n.125-66A>G
ENST00000591658.5:c.398-66A>G ENSP00000477931.1:n.398-66A>G
ENST00000593239.5:c.*62-66A>G ENSP00000484975.1:n.*62-66A>G
ENST00000617460.1:c.398-66A>G ENSP00000481958.1:n.398-66A>G
XM_011525323.1:c.-92-66A>G XP_011523625.1:n.-92-66A>G
XM_011525324.1:c.398-66A>G XP_011523626.1:n.398-66A>G