Canonical Allele Identifier: CA404121378
Community Standard Title: NM_145045.5(ODAD3):c.1116+1G>T
Gene: ODAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11423876C>A , CM000681.2:g.11423876C>A GRCh38
NC_000019.9:g.11534545C>A , CM000681.1:g.11534545C>A GRCh37
NC_000019.8:g.11395545C>A NCBI36
NG_041777.1:g.16907G>T

Transcript Alleles

HGVS Amino-acid Change
NM_145045.5:c.1116+1G>T MANE Select NP_659482.3:n.1116+1G>T
ENST00000356392.9:c.1116+1G>T MANE Select ENSP00000348757.3:n.1116+1G>T
NM_001302453.1:c.954+1G>T NP_001289382.1:n.954+1G>T
NM_001302454.1:c.936+1G>T NP_001289383.1:n.936+1G>T
NM_001302454.2:c.936+1G>T NP_001289383.1:n.936+1G>T
NM_145045.4:c.1116+1G>T NP_659482.3:n.1116+1G>T
ENST00000356392.8:c.1116+1G>T ENSP00000348757.3:n.1116+1G>T
ENST00000586836.5:c.543+1G>T ENSP00000467429.1:n.543+1G>T
ENST00000591179.5:c.936+1G>T ENSP00000466800.1:n.936+1G>T
ENST00000591345.5:c.*1035+1G>T ENSP00000467313.1:n.*1035+1G>T
XM_017026241.1:c.*10+1G>T XP_016881730.1:n.*10+1G>T