Canonical Allele Identifier: CA5453820

Gene: ODAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27985204T>C , CM000672.2:g.27985204T>C	GRCh38
NC_000010.10:g.28274133T>C , CM000672.1:g.28274133T>C	GRCh37
NC_000010.9:g.28314139T>C	NCBI36
NG_042820.1:g.18847A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018076.5:c.390A>G MANE Select	NP_060546.2:p.Arg130=
ENST00000305242.10:c.390A>G MANE Select	ENSP00000306410.5:p.Arg130=
NM_001290020.1:c.390A>G	NP_001276949.1:p.Arg130=
NM_001290020.2:c.390A>G	NP_001276949.1:p.Arg130=
NM_018076.3:c.390A>G	NP_060546.2:p.Arg130=
NM_018076.4:c.390A>G	NP_060546.2:p.Arg130=
ENST00000305242.9:c.390A>G	ENSP00000306410.5:p.Arg130=
ENST00000434029.1:c.72A>G	ENSP00000398155.1:p.Arg24=
ENST00000673439.1:c.390A>G	ENSP00000500782.1:p.Arg130=
XM_011519526.1:c.390A>G	XP_011517828.1:p.Arg130=
XM_011519527.1:c.390A>G	XP_011517829.1:p.Arg130=
XM_011519528.1:c.390A>G	XP_011517830.1:p.Arg130=
XM_011519529.1:c.390A>G	XP_011517831.1:p.Arg130=
XM_011519530.1:c.390A>G	XP_011517832.1:p.Arg130=
XM_011519531.1:c.390A>G	XP_011517833.1:p.Arg130=
XM_011519532.1:c.390A>G	XP_011517834.1:p.Arg130=
XM_011519536.1:c.390A>G	XP_011517838.1:p.Arg130=
XM_017016371.1:c.390A>G	XP_016871860.1:p.Arg130=
XM_024448049.1:c.390A>G	XP_024303817.1:p.Arg130=
XM_024448050.1:c.390A>G	XP_024303818.1:p.Arg130=
XM_024448051.1:c.390A>G	XP_024303819.1:p.Arg130=
XM_024448052.1:c.390A>G	XP_024303820.1:p.Arg130=
XM_024448053.1:c.390A>G	XP_024303821.1:p.Arg130=
XM_024448054.1:c.390A>G	XP_024303822.1:p.Arg130=
XR_002957065.1:n.86+1923T>C