Canonical Allele Identifier: CA376492693
Gene: ODAD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2563330
ClinVar RCV Id: RCV003301491
dbSNP Id: rs1219362986

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27862570T>C , CM000672.2:g.27862570T>C GRCh38
NC_000010.10:g.28151499T>C , CM000672.1:g.28151499T>C GRCh37
NC_000010.9:g.28191505T>C NCBI36
NG_042820.1:g.141481A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305242.10:c.2663A>G MANE Select ENSP00000306410.5:p.Asn888Ser
ENST00000672841.1:c.1739A>G ENSP00000499983.1:p.Asn580Ser
ENST00000672877.1:c.1238A>G ENSP00000500120.1:p.Asn413Ser
ENST00000673384.1:c.1739A>G ENSP00000500856.1:p.Asn580Ser
ENST00000673439.1:c.2663A>G ENSP00000500782.1:p.Asn888Ser
ENST00000305242.9:c.2663A>G ENSP00000306410.5:p.Asn888Ser
NM_001290020.1:c.2663A>G NP_001276949.1:p.Asn888Ser
NM_001290021.1:c.1238A>G NP_001276950.1:p.Asn413Ser
NM_001312689.1:c.1739A>G NP_001299618.1:p.Asn580Ser
NM_018076.3:c.2663A>G NP_060546.2:p.Asn888Ser
NM_018076.4:c.2663A>G NP_060546.2:p.Asn888Ser
XM_011519526.1:c.2663A>G XP_011517828.1:p.Asn888Ser
XM_011519527.1:c.2663A>G XP_011517829.1:p.Asn888Ser
XM_011519528.1:c.2663A>G XP_011517830.1:p.Asn888Ser
XM_011519529.1:c.2663A>G XP_011517831.1:p.Asn888Ser
XM_011519530.1:c.2663A>G XP_011517832.1:p.Asn888Ser
XM_011519531.1:c.2663A>G XP_011517833.1:p.Asn888Ser
XM_011519532.1:c.2453A>G XP_011517834.1:p.Asn818Ser
XM_011519533.1:c.1739A>G XP_011517835.1:p.Asn580Ser
XM_011519534.1:c.1739A>G XP_011517836.1:p.Asn580Ser
XM_011519535.1:c.1577A>G XP_011517837.1:p.Asn526Ser
XM_011519537.1:c.1238A>G XP_011517839.1:p.Asn413Ser
XM_024448049.1:c.2792A>G XP_024303817.1:p.Asn931Ser
XM_024448050.1:c.2792A>G XP_024303818.1:p.Asn931Ser
XM_024448051.1:c.2792A>G XP_024303819.1:p.Asn931Ser
XM_024448052.1:c.2792A>G XP_024303820.1:p.Asn931Ser
XM_024448053.1:c.2792A>G XP_024303821.1:p.Asn931Ser
XM_024448054.1:c.2582A>G XP_024303822.1:p.Asn861Ser
XM_024448055.1:c.1868A>G XP_024303823.1:p.Asn623Ser
XM_024448056.1:c.1868A>G XP_024303824.1:p.Asn623Ser
XM_024448057.1:c.1706A>G XP_024303825.1:p.Asn569Ser
XM_024448058.1:c.1367A>G XP_024303826.1:p.Asn456Ser
NM_001290020.2:c.2663A>G NP_001276949.1:p.Asn888Ser
NM_001290021.2:c.1238A>G NP_001276950.1:p.Asn413Ser
NM_001312689.2:c.1739A>G NP_001299618.1:p.Asn580Ser
NM_018076.5:c.2663A>G MANE Select NP_060546.2:p.Asn888Ser