Canonical Allele Identifier: CA376492546

Gene: ODAD2

Linked Data

• ClinVar Variation Id: 1918920
• ClinVar RCV Id: RCV002594557
• gnomAD v4: 10-27862502-C-A
• COSMIC: COSM2134683 ; COSM4176956
• MyVariant Identifiers: chr10:g.28151431C>A (hg19) ; chr10:g.27862502C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862502C>A , CM000672.2:g.27862502C>A	GRCh38
NC_000010.10:g.28151431C>A , CM000672.1:g.28151431C>A	GRCh37
NC_000010.9:g.28191437C>A	NCBI36
NG_042820.1:g.141549G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2731G>T MANE Select	ENSP00000306410.5:p.Asp911Tyr
ENST00000672841.1:c.1807G>T	ENSP00000499983.1:p.Asp603Tyr
ENST00000672877.1:c.1306G>T	ENSP00000500120.1:p.Asp436Tyr
ENST00000673384.1:c.1807G>T	ENSP00000500856.1:p.Asp603Tyr
ENST00000673439.1:c.2731G>T	ENSP00000500782.1:p.Asp911Tyr
ENST00000305242.9:c.2731G>T	ENSP00000306410.5:p.Asp911Tyr
NM_001290020.1:c.2731G>T	NP_001276949.1:p.Asp911Tyr
NM_001290021.1:c.1306G>T	NP_001276950.1:p.Asp436Tyr
NM_001312689.1:c.1807G>T	NP_001299618.1:p.Asp603Tyr
NM_018076.3:c.2731G>T	NP_060546.2:p.Asp911Tyr
NM_018076.4:c.2731G>T	NP_060546.2:p.Asp911Tyr
XM_011519526.1:c.2731G>T	XP_011517828.1:p.Asp911Tyr
XM_011519527.1:c.2731G>T	XP_011517829.1:p.Asp911Tyr
XM_011519528.1:c.2731G>T	XP_011517830.1:p.Asp911Tyr
XM_011519529.1:c.2731G>T	XP_011517831.1:p.Asp911Tyr
XM_011519530.1:c.2731G>T	XP_011517832.1:p.Asp911Tyr
XM_011519531.1:c.2731G>T	XP_011517833.1:p.Asp911Tyr
XM_011519532.1:c.2521G>T	XP_011517834.1:p.Asp841Tyr
XM_011519533.1:c.1807G>T	XP_011517835.1:p.Asp603Tyr
XM_011519534.1:c.1807G>T	XP_011517836.1:p.Asp603Tyr
XM_011519535.1:c.1645G>T	XP_011517837.1:p.Asp549Tyr
XM_011519537.1:c.1306G>T	XP_011517839.1:p.Asp436Tyr
XM_024448049.1:c.2860G>T	XP_024303817.1:p.Asp954Tyr
XM_024448050.1:c.2860G>T	XP_024303818.1:p.Asp954Tyr
XM_024448051.1:c.2860G>T	XP_024303819.1:p.Asp954Tyr
XM_024448052.1:c.2860G>T	XP_024303820.1:p.Asp954Tyr
XM_024448053.1:c.2860G>T	XP_024303821.1:p.Asp954Tyr
XM_024448054.1:c.2650G>T	XP_024303822.1:p.Asp884Tyr
XM_024448055.1:c.1936G>T	XP_024303823.1:p.Asp646Tyr
XM_024448056.1:c.1936G>T	XP_024303824.1:p.Asp646Tyr
XM_024448057.1:c.1774G>T	XP_024303825.1:p.Asp592Tyr
XM_024448058.1:c.1435G>T	XP_024303826.1:p.Asp479Tyr
NM_001290020.2:c.2731G>T	NP_001276949.1:p.Asp911Tyr
NM_001290021.2:c.1306G>T	NP_001276950.1:p.Asp436Tyr
NM_001312689.2:c.1807G>T	NP_001299618.1:p.Asp603Tyr
NM_018076.5:c.2731G>T MANE Select	NP_060546.2:p.Asp911Tyr