Canonical Allele Identifier: CA404120525

Gene: ODAD3

Linked Data

• gnomAD v4: 19-11422836-T-G
• MyVariant Identifiers: chr19:g.11533504T>G (hg19) ; chr19:g.11422836T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422836T>G , CM000681.2:g.11422836T>G	GRCh38
NC_000019.9:g.11533504T>G , CM000681.1:g.11533504T>G	GRCh37
NC_000019.8:g.11394504T>G	NCBI36
NG_041777.1:g.17947A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1142A>C MANE Select	ENSP00000348757.3:p.Gln381Pro
ENST00000356392.8:c.1142A>C	ENSP00000348757.3:p.Gln381Pro
ENST00000586836.5:c.569A>C	ENSP00000467429.1:p.Gln190Pro
ENST00000591179.5:c.962A>C	ENSP00000466800.1:p.Gln321Pro
ENST00000591345.5:c.*1061A>C	ENSP00000467313.1:n.*1061A>C
NM_001302453.1:c.980A>C	NP_001289382.1:p.Gln327Pro
NM_001302454.1:c.962A>C	NP_001289383.1:p.Gln321Pro
NM_145045.4:c.1142A>C	NP_659482.3:p.Gln381Pro
XM_017026241.1:c.*36A>C	XP_016881730.1:n.*36A>C
NM_145045.5:c.1142A>C MANE Select	NP_659482.3:p.Gln381Pro
NM_001302454.2:c.962A>C	NP_001289383.1:p.Gln321Pro