Canonical Allele Identifier: CA5453591

Gene: ODAD2

Linked Data

• ClinVar Variation Id: 474572
• ClinVar RCV Id: RCV000544285 ; RCV002461332
• dbSNP Id: rs143513621
• ExAC: 10:28250606 C / T
• gnomAD v2: 10-28250606-C-T
• gnomAD v3: 10-27961677-C-T
• gnomAD v4: 10-27961677-C-T
• MyVariant Identifiers: chr10:g.28250606C>T (hg19) ; chr10:g.27961677C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27961677C>T , CM000672.2:g.27961677C>T	GRCh38
NC_000010.10:g.28250606C>T , CM000672.1:g.28250606C>T	GRCh37
NC_000010.9:g.28290612C>T	NCBI36
NG_042820.1:g.42374G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.1277G>A MANE Select	ENSP00000306410.5:p.Ser426Asn
ENST00000672841.1:c.353G>A	ENSP00000499983.1:p.Ser118Asn
ENST00000672877.1:c.-149G>A	ENSP00000500120.1:n.-149G>A
ENST00000673384.1:c.353G>A	ENSP00000500856.1:p.Ser118Asn
ENST00000673439.1:c.1277G>A	ENSP00000500782.1:p.Ser426Asn
ENST00000305242.9:c.1277G>A	ENSP00000306410.5:p.Ser426Asn
ENST00000434029.1:c.959G>A	ENSP00000398155.1:p.Ser320Asn
ENST00000480504.1:n.534G>A
NM_001290020.1:c.1277G>A	NP_001276949.1:p.Ser426Asn
NM_001290021.1:c.-149G>A	NP_001276950.1:n.-149G>A
NM_001312689.1:c.353G>A	NP_001299618.1:p.Ser118Asn
NM_018076.3:c.1277G>A	NP_060546.2:p.Ser426Asn
NM_018076.4:c.1277G>A	NP_060546.2:p.Ser426Asn
XM_011519526.1:c.1277G>A	XP_011517828.1:p.Ser426Asn
XM_011519527.1:c.1277G>A	XP_011517829.1:p.Ser426Asn
XM_011519528.1:c.1277G>A	XP_011517830.1:p.Ser426Asn
XM_011519529.1:c.1277G>A	XP_011517831.1:p.Ser426Asn
XM_011519530.1:c.1277G>A	XP_011517832.1:p.Ser426Asn
XM_011519531.1:c.1277G>A	XP_011517833.1:p.Ser426Asn
XM_011519532.1:c.1277G>A	XP_011517834.1:p.Ser426Asn
XM_011519533.1:c.353G>A	XP_011517835.1:p.Ser118Asn
XM_011519534.1:c.353G>A	XP_011517836.1:p.Ser118Asn
XM_011519535.1:c.191G>A	XP_011517837.1:p.Ser64Asn
XM_011519536.1:c.1277G>A	XP_011517838.1:p.Ser426Asn
XM_017016371.1:c.1277G>A	XP_016871860.1:p.Ser426Asn
XM_024448049.1:c.1277G>A	XP_024303817.1:p.Ser426Asn
XM_024448050.1:c.1277G>A	XP_024303818.1:p.Ser426Asn
XM_024448051.1:c.1277G>A	XP_024303819.1:p.Ser426Asn
XM_024448052.1:c.1277G>A	XP_024303820.1:p.Ser426Asn
XM_024448053.1:c.1277G>A	XP_024303821.1:p.Ser426Asn
XM_024448054.1:c.1277G>A	XP_024303822.1:p.Ser426Asn
XM_024448055.1:c.353G>A	XP_024303823.1:p.Ser118Asn
XM_024448056.1:c.353G>A	XP_024303824.1:p.Ser118Asn
XM_024448057.1:c.191G>A	XP_024303825.1:p.Ser64Asn
NM_001290020.2:c.1277G>A	NP_001276949.1:p.Ser426Asn
NM_001290021.2:c.-149G>A	NP_001276950.1:n.-149G>A
NM_001312689.2:c.353G>A	NP_001299618.1:p.Ser118Asn
NM_018076.5:c.1277G>A MANE Select	NP_060546.2:p.Ser426Asn