Canonical Allele Identifier: CA376393848

Gene: ODAD2

Linked Data

• ClinVar Variation Id: 541494
• ClinVar RCV Id: RCV000651794
• dbSNP Id: rs1554822213
• MyVariant Identifiers: chr10:g.28257948C>A (hg19) ; chr10:g.27969019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27969019C>A , CM000672.2:g.27969019C>A	GRCh38
NC_000010.10:g.28257948C>A , CM000672.1:g.28257948C>A	GRCh37
NC_000010.9:g.28297954C>A	NCBI36
NG_042820.1:g.35032G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.1143-1G>T MANE Select	ENSP00000306410.5:n.1143-1G>T
ENST00000672841.1:c.219-1G>T	ENSP00000499983.1:n.219-1G>T
ENST00000672877.1:c.-187-7304G>T	ENSP00000500120.1:n.-187-7304G>T
ENST00000673384.1:c.219-1G>T	ENSP00000500856.1:n.219-1G>T
ENST00000673439.1:c.1143-1G>T	ENSP00000500782.1:n.1143-1G>T
ENST00000673512.1:c.219-1G>T	ENSP00000499923.1:n.219-1G>T
ENST00000305242.9:c.1143-1G>T	ENSP00000306410.5:n.1143-1G>T
ENST00000434029.1:c.825-1G>T	ENSP00000398155.1:n.825-1G>T
ENST00000480504.1:n.400-1G>T
NM_001290020.1:c.1143-1G>T	NP_001276949.1:n.1143-1G>T
NM_001290021.1:c.-187-7304G>T	NP_001276950.1:n.-187-7304G>T
NM_001312689.1:c.219-1G>T	NP_001299618.1:n.219-1G>T
NM_018076.3:c.1143-1G>T	NP_060546.2:n.1143-1G>T
NM_018076.4:c.1143-1G>T	NP_060546.2:n.1143-1G>T
XM_011519526.1:c.1143-1G>T	XP_011517828.1:n.1143-1G>T
XM_011519527.1:c.1143-1G>T	XP_011517829.1:n.1143-1G>T
XM_011519528.1:c.1143-1G>T	XP_011517830.1:n.1143-1G>T
XM_011519529.1:c.1143-1G>T	XP_011517831.1:n.1143-1G>T
XM_011519530.1:c.1143-1G>T	XP_011517832.1:n.1143-1G>T
XM_011519531.1:c.1143-1G>T	XP_011517833.1:n.1143-1G>T
XM_011519532.1:c.1143-1G>T	XP_011517834.1:n.1143-1G>T
XM_011519533.1:c.219-1G>T	XP_011517835.1:n.219-1G>T
XM_011519534.1:c.219-1G>T	XP_011517836.1:n.219-1G>T
XM_011519535.1:c.57-1G>T	XP_011517837.1:n.57-1G>T
XM_011519536.1:c.1143-1G>T	XP_011517838.1:n.1143-1G>T
XM_017016371.1:c.1143-1G>T	XP_016871860.1:n.1143-1G>T
XM_024448049.1:c.1143-1G>T	XP_024303817.1:n.1143-1G>T
XM_024448050.1:c.1143-1G>T	XP_024303818.1:n.1143-1G>T
XM_024448051.1:c.1143-1G>T	XP_024303819.1:n.1143-1G>T
XM_024448052.1:c.1143-1G>T	XP_024303820.1:n.1143-1G>T
XM_024448053.1:c.1143-1G>T	XP_024303821.1:n.1143-1G>T
XM_024448054.1:c.1143-1G>T	XP_024303822.1:n.1143-1G>T
XM_024448055.1:c.219-1G>T	XP_024303823.1:n.219-1G>T
XM_024448056.1:c.219-1G>T	XP_024303824.1:n.219-1G>T
XM_024448057.1:c.57-1G>T	XP_024303825.1:n.57-1G>T
NM_001290020.2:c.1143-1G>T	NP_001276949.1:n.1143-1G>T
NM_001290021.2:c.-187-7304G>T	NP_001276950.1:n.-187-7304G>T
NM_001312689.2:c.219-1G>T	NP_001299618.1:n.219-1G>T
NM_018076.5:c.1143-1G>T MANE Select	NP_060546.2:n.1143-1G>T