Canonical Allele Identifier: CA505749501
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533467G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422799G>A , CM000681.2:g.11422799G>A GRCh38
NC_000019.9:g.11533467G>A , CM000681.1:g.11533467G>A GRCh37
NC_000019.8:g.11394467G>A NCBI36
NG_041777.1:g.17984C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1179C>T MANE Select ENSP00000348757.3:p.Ser393=
ENST00000356392.8:c.1179C>T ENSP00000348757.3:p.Ser393=
ENST00000586836.5:c.606C>T ENSP00000467429.1:p.Ser202=
ENST00000591179.5:c.999C>T ENSP00000466800.1:p.Ser333=
ENST00000591345.5:c.*1098C>T ENSP00000467313.1:n.*1098C>T
NM_001302453.1:c.1017C>T NP_001289382.1:p.Ser339=
NM_001302454.1:c.999C>T NP_001289383.1:p.Ser333=
NM_145045.4:c.1179C>T NP_659482.3:p.Ser393=
XM_017026241.1:c.*73C>T XP_016881730.1:n.*73C>T
NM_145045.5:c.1179C>T MANE Select NP_659482.3:p.Ser393=
NM_001302454.2:c.999C>T NP_001289383.1:p.Ser333=