Canonical Allele Identifier: CA214699
Gene: ODAD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 66047
ClinVar RCV Id: RCV000056286
dbSNP Id: rs587777049

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27862558G>T , CM000672.2:g.27862558G>T GRCh38
NC_000010.10:g.28151487G>T , CM000672.1:g.28151487G>T GRCh37
NC_000010.9:g.28191493G>T NCBI36
NG_042820.1:g.141493C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305242.10:c.2675C>A MANE Select ENSP00000306410.5:p.Ser892Ter
ENST00000672841.1:c.1751C>A ENSP00000499983.1:p.Ser584Ter
ENST00000672877.1:c.1250C>A ENSP00000500120.1:p.Ser417Ter
ENST00000673384.1:c.1751C>A ENSP00000500856.1:p.Ser584Ter
ENST00000673439.1:c.2675C>A ENSP00000500782.1:p.Ser892Ter
ENST00000305242.9:c.2675C>A ENSP00000306410.5:p.Ser892Ter
NM_001290020.1:c.2675C>A NP_001276949.1:p.Ser892Ter
NM_001290021.1:c.1250C>A NP_001276950.1:p.Ser417Ter
NM_001312689.1:c.1751C>A NP_001299618.1:p.Ser584Ter
NM_018076.3:c.2675C>A NP_060546.2:p.Ser892Ter
NM_018076.4:c.2675C>A NP_060546.2:p.Ser892Ter
XM_011519526.1:c.2675C>A XP_011517828.1:p.Ser892Ter
XM_011519527.1:c.2675C>A XP_011517829.1:p.Ser892Ter
XM_011519528.1:c.2675C>A XP_011517830.1:p.Ser892Ter
XM_011519529.1:c.2675C>A XP_011517831.1:p.Ser892Ter
XM_011519530.1:c.2675C>A XP_011517832.1:p.Ser892Ter
XM_011519531.1:c.2675C>A XP_011517833.1:p.Ser892Ter
XM_011519532.1:c.2465C>A XP_011517834.1:p.Ser822Ter
XM_011519533.1:c.1751C>A XP_011517835.1:p.Ser584Ter
XM_011519534.1:c.1751C>A XP_011517836.1:p.Ser584Ter
XM_011519535.1:c.1589C>A XP_011517837.1:p.Ser530Ter
XM_011519537.1:c.1250C>A XP_011517839.1:p.Ser417Ter
XM_024448049.1:c.2804C>A XP_024303817.1:p.Ser935Ter
XM_024448050.1:c.2804C>A XP_024303818.1:p.Ser935Ter
XM_024448051.1:c.2804C>A XP_024303819.1:p.Ser935Ter
XM_024448052.1:c.2804C>A XP_024303820.1:p.Ser935Ter
XM_024448053.1:c.2804C>A XP_024303821.1:p.Ser935Ter
XM_024448054.1:c.2594C>A XP_024303822.1:p.Ser865Ter
XM_024448055.1:c.1880C>A XP_024303823.1:p.Ser627Ter
XM_024448056.1:c.1880C>A XP_024303824.1:p.Ser627Ter
XM_024448057.1:c.1718C>A XP_024303825.1:p.Ser573Ter
XM_024448058.1:c.1379C>A XP_024303826.1:p.Ser460Ter
NM_001290020.2:c.2675C>A NP_001276949.1:p.Ser892Ter
NM_001290021.2:c.1250C>A NP_001276950.1:p.Ser417Ter
NM_001312689.2:c.1751C>A NP_001299618.1:p.Ser584Ter
NM_018076.5:c.2675C>A MANE Select NP_060546.2:p.Ser892Ter