Canonical Allele Identifier: CA404120487

Gene: ODAD3

Linked Data

• gnomAD v4: 19-11422828-T-A
• MyVariant Identifiers: chr19:g.11533496T>A (hg19) ; chr19:g.11422828T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422828T>A , CM000681.2:g.11422828T>A	GRCh38
NC_000019.9:g.11533496T>A , CM000681.1:g.11533496T>A	GRCh37
NC_000019.8:g.11394496T>A	NCBI36
NG_041777.1:g.17955A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1150A>T MANE Select	ENSP00000348757.3:p.Thr384Ser
ENST00000356392.8:c.1150A>T	ENSP00000348757.3:p.Thr384Ser
ENST00000586836.5:c.577A>T	ENSP00000467429.1:p.Thr193Ser
ENST00000591179.5:c.970A>T	ENSP00000466800.1:p.Thr324Ser
ENST00000591345.5:c.*1069A>T	ENSP00000467313.1:n.*1069A>T
NM_001302453.1:c.988A>T	NP_001289382.1:p.Thr330Ser
NM_001302454.1:c.970A>T	NP_001289383.1:p.Thr324Ser
NM_145045.4:c.1150A>T	NP_659482.3:p.Thr384Ser
XM_017026241.1:c.*44A>T	XP_016881730.1:n.*44A>T
NM_145045.5:c.1150A>T MANE Select	NP_659482.3:p.Thr384Ser
NM_001302454.2:c.970A>T	NP_001289383.1:p.Thr324Ser