Canonical Allele Identifier: CA214765

Gene: ODAD2

Linked Data

• ClinVar Variation Id: 66045
• ClinVar RCV Id: RCV000056284 ; RCV000190922
• dbSNP Id: rs587777047
• gnomAD v4: 10-27862453-A-C
• MyVariant Identifiers: chr10:g.28151382A>C (hg19) ; chr10:g.27862453A>C (hg38)
• PubMed: PMID:20301301 ; PMID:23849778

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862453A>C , CM000672.2:g.27862453A>C	GRCh38
NC_000010.10:g.28151382A>C , CM000672.1:g.28151382A>C	GRCh37
NC_000010.9:g.28191388A>C	NCBI36
NG_042820.1:g.141598T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2780T>G MANE Select	ENSP00000306410.5:p.Leu927Trp
ENST00000672841.1:c.1856T>G	ENSP00000499983.1:p.Leu619Trp
ENST00000672877.1:c.1355T>G	ENSP00000500120.1:p.Leu452Trp
ENST00000673384.1:c.1856T>G	ENSP00000500856.1:p.Leu619Trp
ENST00000673439.1:c.2780T>G	ENSP00000500782.1:p.Leu927Trp
ENST00000305242.9:c.2780T>G	ENSP00000306410.5:p.Leu927Trp
NM_001290020.1:c.2780T>G	NP_001276949.1:p.Leu927Trp
NM_001290021.1:c.1355T>G	NP_001276950.1:p.Leu452Trp
NM_001312689.1:c.1856T>G	NP_001299618.1:p.Leu619Trp
NM_018076.3:c.2780T>G	NP_060546.2:p.Leu927Trp
NM_018076.4:c.2780T>G	NP_060546.2:p.Leu927Trp
XM_011519526.1:c.2780T>G	XP_011517828.1:p.Leu927Trp
XM_011519527.1:c.2780T>G	XP_011517829.1:p.Leu927Trp
XM_011519528.1:c.2780T>G	XP_011517830.1:p.Leu927Trp
XM_011519529.1:c.2780T>G	XP_011517831.1:p.Leu927Trp
XM_011519530.1:c.2780T>G	XP_011517832.1:p.Leu927Trp
XM_011519531.1:c.2780T>G	XP_011517833.1:p.Leu927Trp
XM_011519532.1:c.2570T>G	XP_011517834.1:p.Leu857Trp
XM_011519533.1:c.1856T>G	XP_011517835.1:p.Leu619Trp
XM_011519534.1:c.1856T>G	XP_011517836.1:p.Leu619Trp
XM_011519535.1:c.1694T>G	XP_011517837.1:p.Leu565Trp
XM_011519537.1:c.1355T>G	XP_011517839.1:p.Leu452Trp
XM_024448049.1:c.2909T>G	XP_024303817.1:p.Leu970Trp
XM_024448050.1:c.2909T>G	XP_024303818.1:p.Leu970Trp
XM_024448051.1:c.2909T>G	XP_024303819.1:p.Leu970Trp
XM_024448052.1:c.2909T>G	XP_024303820.1:p.Leu970Trp
XM_024448053.1:c.2909T>G	XP_024303821.1:p.Leu970Trp
XM_024448054.1:c.2699T>G	XP_024303822.1:p.Leu900Trp
XM_024448055.1:c.1985T>G	XP_024303823.1:p.Leu662Trp
XM_024448056.1:c.1985T>G	XP_024303824.1:p.Leu662Trp
XM_024448057.1:c.1823T>G	XP_024303825.1:p.Leu608Trp
XM_024448058.1:c.1484T>G	XP_024303826.1:p.Leu495Trp
NM_001290020.2:c.2780T>G	NP_001276949.1:p.Leu927Trp
NM_001290021.2:c.1355T>G	NP_001276950.1:p.Leu452Trp
NM_001312689.2:c.1856T>G	NP_001299618.1:p.Leu619Trp
NM_018076.5:c.2780T>G MANE Select	NP_060546.2:p.Leu927Trp