Canonical Allele Identifier: CA376492764

Gene: ODAD2

Linked Data

• MyVariant Identifiers: chr10:g.28151535A>T (hg19) ; chr10:g.27862606A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862606A>T , CM000672.2:g.27862606A>T	GRCh38
NC_000010.10:g.28151535A>T , CM000672.1:g.28151535A>T	GRCh37
NC_000010.9:g.28191541A>T	NCBI36
NG_042820.1:g.141445T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2627T>A MANE Select	ENSP00000306410.5:p.Val876Asp
ENST00000672841.1:c.1703T>A	ENSP00000499983.1:p.Val568Asp
ENST00000672877.1:c.1202T>A	ENSP00000500120.1:p.Val401Asp
ENST00000673384.1:c.1703T>A	ENSP00000500856.1:p.Val568Asp
ENST00000673439.1:c.2627T>A	ENSP00000500782.1:p.Val876Asp
ENST00000305242.9:c.2627T>A	ENSP00000306410.5:p.Val876Asp
NM_001290020.1:c.2627T>A	NP_001276949.1:p.Val876Asp
NM_001290021.1:c.1202T>A	NP_001276950.1:p.Val401Asp
NM_001312689.1:c.1703T>A	NP_001299618.1:p.Val568Asp
NM_018076.3:c.2627T>A	NP_060546.2:p.Val876Asp
NM_018076.4:c.2627T>A	NP_060546.2:p.Val876Asp
XM_011519526.1:c.2627T>A	XP_011517828.1:p.Val876Asp
XM_011519527.1:c.2627T>A	XP_011517829.1:p.Val876Asp
XM_011519528.1:c.2627T>A	XP_011517830.1:p.Val876Asp
XM_011519529.1:c.2627T>A	XP_011517831.1:p.Val876Asp
XM_011519530.1:c.2627T>A	XP_011517832.1:p.Val876Asp
XM_011519531.1:c.2627T>A	XP_011517833.1:p.Val876Asp
XM_011519532.1:c.2417T>A	XP_011517834.1:p.Val806Asp
XM_011519533.1:c.1703T>A	XP_011517835.1:p.Val568Asp
XM_011519534.1:c.1703T>A	XP_011517836.1:p.Val568Asp
XM_011519535.1:c.1541T>A	XP_011517837.1:p.Val514Asp
XM_011519537.1:c.1202T>A	XP_011517839.1:p.Val401Asp
XM_024448049.1:c.2756T>A	XP_024303817.1:p.Val919Asp
XM_024448050.1:c.2756T>A	XP_024303818.1:p.Val919Asp
XM_024448051.1:c.2756T>A	XP_024303819.1:p.Val919Asp
XM_024448052.1:c.2756T>A	XP_024303820.1:p.Val919Asp
XM_024448053.1:c.2756T>A	XP_024303821.1:p.Val919Asp
XM_024448054.1:c.2546T>A	XP_024303822.1:p.Val849Asp
XM_024448055.1:c.1832T>A	XP_024303823.1:p.Val611Asp
XM_024448056.1:c.1832T>A	XP_024303824.1:p.Val611Asp
XM_024448057.1:c.1670T>A	XP_024303825.1:p.Val557Asp
XM_024448058.1:c.1331T>A	XP_024303826.1:p.Val444Asp
NM_001290020.2:c.2627T>A	NP_001276949.1:p.Val876Asp
NM_001290021.2:c.1202T>A	NP_001276950.1:p.Val401Asp
NM_001312689.2:c.1703T>A	NP_001299618.1:p.Val568Asp
NM_018076.5:c.2627T>A MANE Select	NP_060546.2:p.Val876Asp