Canonical Allele Identifier: CA10584010

Gene: ODAD2

Linked Data

• ClinVar Variation Id: 242857
• ClinVar RCV Id: RCV000234915 ; RCV000608160
• dbSNP Id: rs879253744
• gnomAD v2: 10-28223938-C-T
• gnomAD v4: 10-27935009-C-T
• MyVariant Identifiers: chr10:g.28223938C>T (hg19) ; chr10:g.27935009C>T (hg38)
• PubMed: PMID:23849778

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27935009C>T , CM000672.2:g.27935009C>T	GRCh38
NC_000010.10:g.28223938C>T , CM000672.1:g.28223938C>T	GRCh37
NC_000010.9:g.28263944C>T	NCBI36
NG_042820.1:g.69042G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2495+1G>A MANE Select	ENSP00000306410.5:n.2495+1G>A
ENST00000672841.1:c.1571+1G>A	ENSP00000499983.1:n.1571+1G>A
ENST00000672877.1:c.1070+1G>A	ENSP00000500120.1:n.1070+1G>A
ENST00000673384.1:c.1571+1G>A	ENSP00000500856.1:n.1571+1G>A
ENST00000673439.1:c.2495+1G>A	ENSP00000500782.1:n.2495+1G>A
ENST00000305242.9:c.2495+1G>A	ENSP00000306410.5:n.2495+1G>A
NM_001290020.1:c.2495+1G>A	NP_001276949.1:n.2495+1G>A
NM_001290021.1:c.1070+1G>A	NP_001276950.1:n.1070+1G>A
NM_001312689.1:c.1571+1G>A	NP_001299618.1:n.1571+1G>A
NM_018076.3:c.2495+1G>A	NP_060546.2:n.2495+1G>A
NM_018076.4:c.2495+1G>A	NP_060546.2:n.2495+1G>A
XM_011519526.1:c.2495+1G>A	XP_011517828.1:n.2495+1G>A
XM_011519527.1:c.2495+1G>A	XP_011517829.1:n.2495+1G>A
XM_011519528.1:c.2495+1G>A	XP_011517830.1:n.2495+1G>A
XM_011519529.1:c.2495+1G>A	XP_011517831.1:n.2495+1G>A
XM_011519530.1:c.2495+1G>A	XP_011517832.1:n.2495+1G>A
XM_011519531.1:c.2495+1G>A	XP_011517833.1:n.2495+1G>A
XM_011519532.1:c.2285+1G>A	XP_011517834.1:n.2285+1G>A
XM_011519533.1:c.1571+1G>A	XP_011517835.1:n.1571+1G>A
XM_011519534.1:c.1571+1G>A	XP_011517836.1:n.1571+1G>A
XM_011519535.1:c.1409+1G>A	XP_011517837.1:n.1409+1G>A
XM_011519537.1:c.1070+1G>A	XP_011517839.1:n.1070+1G>A
XM_024448049.1:c.2495+1G>A	XP_024303817.1:n.2495+1G>A
XM_024448050.1:c.2495+1G>A	XP_024303818.1:n.2495+1G>A
XM_024448051.1:c.2495+1G>A	XP_024303819.1:n.2495+1G>A
XM_024448052.1:c.2495+1G>A	XP_024303820.1:n.2495+1G>A
XM_024448053.1:c.2495+1G>A	XP_024303821.1:n.2495+1G>A
XM_024448054.1:c.2285+1G>A	XP_024303822.1:n.2285+1G>A
XM_024448055.1:c.1571+1G>A	XP_024303823.1:n.1571+1G>A
XM_024448056.1:c.1571+1G>A	XP_024303824.1:n.1571+1G>A
XM_024448057.1:c.1409+1G>A	XP_024303825.1:n.1409+1G>A
XM_024448058.1:c.1070+1G>A	XP_024303826.1:n.1070+1G>A
NM_001290020.2:c.2495+1G>A	NP_001276949.1:n.2495+1G>A
NM_001290021.2:c.1070+1G>A	NP_001276950.1:n.1070+1G>A
NM_001312689.2:c.1571+1G>A	NP_001299618.1:n.1571+1G>A
NM_018076.5:c.2495+1G>A MANE Select	NP_060546.2:n.2495+1G>A