Canonical Allele Identifier: CA376492754

Gene: ODAD2

Linked Data

• MyVariant Identifiers: chr10:g.28151527A>C (hg19) ; chr10:g.27862598A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862598A>C , CM000672.2:g.27862598A>C	GRCh38
NC_000010.10:g.28151527A>C , CM000672.1:g.28151527A>C	GRCh37
NC_000010.9:g.28191533A>C	NCBI36
NG_042820.1:g.141453T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2635T>G MANE Select	ENSP00000306410.5:p.Phe879Val
ENST00000672841.1:c.1711T>G	ENSP00000499983.1:p.Phe571Val
ENST00000672877.1:c.1210T>G	ENSP00000500120.1:p.Phe404Val
ENST00000673384.1:c.1711T>G	ENSP00000500856.1:p.Phe571Val
ENST00000673439.1:c.2635T>G	ENSP00000500782.1:p.Phe879Val
ENST00000305242.9:c.2635T>G	ENSP00000306410.5:p.Phe879Val
NM_001290020.1:c.2635T>G	NP_001276949.1:p.Phe879Val
NM_001290021.1:c.1210T>G	NP_001276950.1:p.Phe404Val
NM_001312689.1:c.1711T>G	NP_001299618.1:p.Phe571Val
NM_018076.3:c.2635T>G	NP_060546.2:p.Phe879Val
NM_018076.4:c.2635T>G	NP_060546.2:p.Phe879Val
XM_011519526.1:c.2635T>G	XP_011517828.1:p.Phe879Val
XM_011519527.1:c.2635T>G	XP_011517829.1:p.Phe879Val
XM_011519528.1:c.2635T>G	XP_011517830.1:p.Phe879Val
XM_011519529.1:c.2635T>G	XP_011517831.1:p.Phe879Val
XM_011519530.1:c.2635T>G	XP_011517832.1:p.Phe879Val
XM_011519531.1:c.2635T>G	XP_011517833.1:p.Phe879Val
XM_011519532.1:c.2425T>G	XP_011517834.1:p.Phe809Val
XM_011519533.1:c.1711T>G	XP_011517835.1:p.Phe571Val
XM_011519534.1:c.1711T>G	XP_011517836.1:p.Phe571Val
XM_011519535.1:c.1549T>G	XP_011517837.1:p.Phe517Val
XM_011519537.1:c.1210T>G	XP_011517839.1:p.Phe404Val
XM_024448049.1:c.2764T>G	XP_024303817.1:p.Phe922Val
XM_024448050.1:c.2764T>G	XP_024303818.1:p.Phe922Val
XM_024448051.1:c.2764T>G	XP_024303819.1:p.Phe922Val
XM_024448052.1:c.2764T>G	XP_024303820.1:p.Phe922Val
XM_024448053.1:c.2764T>G	XP_024303821.1:p.Phe922Val
XM_024448054.1:c.2554T>G	XP_024303822.1:p.Phe852Val
XM_024448055.1:c.1840T>G	XP_024303823.1:p.Phe614Val
XM_024448056.1:c.1840T>G	XP_024303824.1:p.Phe614Val
XM_024448057.1:c.1678T>G	XP_024303825.1:p.Phe560Val
XM_024448058.1:c.1339T>G	XP_024303826.1:p.Phe447Val
NM_001290020.2:c.2635T>G	NP_001276949.1:p.Phe879Val
NM_001290021.2:c.1210T>G	NP_001276950.1:p.Phe404Val
NM_001312689.2:c.1711T>G	NP_001299618.1:p.Phe571Val
NM_018076.5:c.2635T>G MANE Select	NP_060546.2:p.Phe879Val