Canonical Allele Identifier: CA2735476075
Gene: ODAD3 HGNC NCBI

Linked Data

dbSNP Id: rs2144756192

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422996_11423001dup , CM000681.2:g.11422996_11423001dup GRCh38
NC_000019.9:g.11533664_11533669dup , CM000681.1:g.11533664_11533669dup GRCh37
NC_000019.8:g.11394664_11394669dup NCBI36
NG_041777.1:g.17782_17787dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1117-140_1117-135dup MANE Select ENSP00000348757.3:n.1117-140_1117-135dup
ENST00000356392.8:c.1117-140_1117-135dup ENSP00000348757.3:n.1117-140_1117-135dup
ENST00000586836.5:c.544-140_544-135dup ENSP00000467429.1:n.544-140_544-135dup
ENST00000591179.5:c.937-140_937-135dup ENSP00000466800.1:n.937-140_937-135dup
ENST00000591345.5:c.*1036-140_*1036-135dup ENSP00000467313.1:n.*1036-140_*1036-135dup
NM_001302453.1:c.955-140_955-135dup NP_001289382.1:n.955-140_955-135dup
NM_001302454.1:c.937-140_937-135dup NP_001289383.1:n.937-140_937-135dup
NM_145045.4:c.1117-140_1117-135dup NP_659482.3:n.1117-140_1117-135dup
XM_017026241.1:c.*11-140_*11-135dup XP_016881730.1:n.*11-140_*11-135dup
NM_145045.5:c.1117-140_1117-135dup MANE Select NP_659482.3:n.1117-140_1117-135dup
NM_001302454.2:c.937-140_937-135dup NP_001289383.1:n.937-140_937-135dup