Canonical Allele Identifier: CA376492798

Gene: ODAD2

Linked Data

• MyVariant Identifiers: chr10:g.28151551C>A (hg19) ; chr10:g.27862622C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862622C>A , CM000672.2:g.27862622C>A	GRCh38
NC_000010.10:g.28151551C>A , CM000672.1:g.28151551C>A	GRCh37
NC_000010.9:g.28191557C>A	NCBI36
NG_042820.1:g.141429G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2611G>T MANE Select	ENSP00000306410.5:p.Asp871Tyr
ENST00000672841.1:c.1687G>T	ENSP00000499983.1:p.Asp563Tyr
ENST00000672877.1:c.1186G>T	ENSP00000500120.1:p.Asp396Tyr
ENST00000673384.1:c.1687G>T	ENSP00000500856.1:p.Asp563Tyr
ENST00000673439.1:c.2611G>T	ENSP00000500782.1:p.Asp871Tyr
ENST00000305242.9:c.2611G>T	ENSP00000306410.5:p.Asp871Tyr
NM_001290020.1:c.2611G>T	NP_001276949.1:p.Asp871Tyr
NM_001290021.1:c.1186G>T	NP_001276950.1:p.Asp396Tyr
NM_001312689.1:c.1687G>T	NP_001299618.1:p.Asp563Tyr
NM_018076.3:c.2611G>T	NP_060546.2:p.Asp871Tyr
NM_018076.4:c.2611G>T	NP_060546.2:p.Asp871Tyr
XM_011519526.1:c.2611G>T	XP_011517828.1:p.Asp871Tyr
XM_011519527.1:c.2611G>T	XP_011517829.1:p.Asp871Tyr
XM_011519528.1:c.2611G>T	XP_011517830.1:p.Asp871Tyr
XM_011519529.1:c.2611G>T	XP_011517831.1:p.Asp871Tyr
XM_011519530.1:c.2611G>T	XP_011517832.1:p.Asp871Tyr
XM_011519531.1:c.2611G>T	XP_011517833.1:p.Asp871Tyr
XM_011519532.1:c.2401G>T	XP_011517834.1:p.Asp801Tyr
XM_011519533.1:c.1687G>T	XP_011517835.1:p.Asp563Tyr
XM_011519534.1:c.1687G>T	XP_011517836.1:p.Asp563Tyr
XM_011519535.1:c.1525G>T	XP_011517837.1:p.Asp509Tyr
XM_011519537.1:c.1186G>T	XP_011517839.1:p.Asp396Tyr
XM_024448049.1:c.2740G>T	XP_024303817.1:p.Asp914Tyr
XM_024448050.1:c.2740G>T	XP_024303818.1:p.Asp914Tyr
XM_024448051.1:c.2740G>T	XP_024303819.1:p.Asp914Tyr
XM_024448052.1:c.2740G>T	XP_024303820.1:p.Asp914Tyr
XM_024448053.1:c.2740G>T	XP_024303821.1:p.Asp914Tyr
XM_024448054.1:c.2530G>T	XP_024303822.1:p.Asp844Tyr
XM_024448055.1:c.1816G>T	XP_024303823.1:p.Asp606Tyr
XM_024448056.1:c.1816G>T	XP_024303824.1:p.Asp606Tyr
XM_024448057.1:c.1654G>T	XP_024303825.1:p.Asp552Tyr
XM_024448058.1:c.1315G>T	XP_024303826.1:p.Asp439Tyr
NM_001290020.2:c.2611G>T	NP_001276949.1:p.Asp871Tyr
NM_001290021.2:c.1186G>T	NP_001276950.1:p.Asp396Tyr
NM_001312689.2:c.1687G>T	NP_001299618.1:p.Asp563Tyr
NM_018076.5:c.2611G>T MANE Select	NP_060546.2:p.Asp871Tyr