Canonical Allele Identifier: CA404120578

Gene: ODAD3

Linked Data

• gnomAD v4: 19-11422852-G-A
• COSMIC: COSM6391452
• MyVariant Identifiers: chr19:g.11533520G>A (hg19) ; chr19:g.11422852G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422852G>A , CM000681.2:g.11422852G>A	GRCh38
NC_000019.9:g.11533520G>A , CM000681.1:g.11533520G>A	GRCh37
NC_000019.8:g.11394520G>A	NCBI36
NG_041777.1:g.17931C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1126C>T MANE Select	ENSP00000348757.3:p.Arg376Trp
ENST00000356392.8:c.1126C>T	ENSP00000348757.3:p.Arg376Trp
ENST00000586836.5:c.553C>T	ENSP00000467429.1:p.Arg185Trp
ENST00000591179.5:c.946C>T	ENSP00000466800.1:p.Arg316Trp
ENST00000591345.5:c.*1045C>T	ENSP00000467313.1:n.*1045C>T
NM_001302453.1:c.964C>T	NP_001289382.1:p.Arg322Trp
NM_001302454.1:c.946C>T	NP_001289383.1:p.Arg316Trp
NM_145045.4:c.1126C>T	NP_659482.3:p.Arg376Trp
XM_017026241.1:c.*20C>T	XP_016881730.1:n.*20C>T
NM_145045.5:c.1126C>T MANE Select	NP_659482.3:p.Arg376Trp
NM_001302454.2:c.946C>T	NP_001289383.1:p.Arg316Trp