Canonical Allele Identifier: CA404120546

Gene: ODAD3

Linked Data

• dbSNP Id: rs1222941936
• gnomAD v2: 19-11533510-A-G
• gnomAD v4: 19-11422842-A-G
• MyVariant Identifiers: chr19:g.11533510A>G (hg19) ; chr19:g.11422842A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422842A>G , CM000681.2:g.11422842A>G	GRCh38
NC_000019.9:g.11533510A>G , CM000681.1:g.11533510A>G	GRCh37
NC_000019.8:g.11394510A>G	NCBI36
NG_041777.1:g.17941T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1136T>C MANE Select	ENSP00000348757.3:p.Leu379Pro
ENST00000356392.8:c.1136T>C	ENSP00000348757.3:p.Leu379Pro
ENST00000586836.5:c.563T>C	ENSP00000467429.1:p.Leu188Pro
ENST00000591179.5:c.956T>C	ENSP00000466800.1:p.Leu319Pro
ENST00000591345.5:c.*1055T>C	ENSP00000467313.1:n.*1055T>C
NM_001302453.1:c.974T>C	NP_001289382.1:p.Leu325Pro
NM_001302454.1:c.956T>C	NP_001289383.1:p.Leu319Pro
NM_145045.4:c.1136T>C	NP_659482.3:p.Leu379Pro
XM_017026241.1:c.*30T>C	XP_016881730.1:n.*30T>C
NM_145045.5:c.1136T>C MANE Select	NP_659482.3:p.Leu379Pro
NM_001302454.2:c.956T>C	NP_001289383.1:p.Leu319Pro