Canonical Allele Identifier: CA5453616
Community Standard Title: NM_018076.5(ODAD2):c.1237C>G (p.Arg413Gly)
Gene: ODAD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27968924G>C , CM000672.2:g.27968924G>C GRCh38
NC_000010.10:g.28257853G>C , CM000672.1:g.28257853G>C GRCh37
NC_000010.9:g.28297859G>C NCBI36
NG_042820.1:g.35127C>G

Transcript Alleles

HGVS Amino-acid Change
NM_018076.5:c.1237C>G MANE Select NP_060546.2:p.Arg413Gly
ENST00000305242.10:c.1237C>G MANE Select ENSP00000306410.5:p.Arg413Gly
NM_001290020.1:c.1237C>G NP_001276949.1:p.Arg413Gly
NM_001290020.2:c.1237C>G NP_001276949.1:p.Arg413Gly
NM_001290021.1:c.-187-7209C>G NP_001276950.1:n.-187-7209C>G
NM_001290021.2:c.-187-7209C>G NP_001276950.1:n.-187-7209C>G
NM_001312689.1:c.313C>G NP_001299618.1:p.Arg105Gly
NM_001312689.2:c.313C>G NP_001299618.1:p.Arg105Gly
NM_018076.3:c.1237C>G NP_060546.2:p.Arg413Gly
NM_018076.4:c.1237C>G NP_060546.2:p.Arg413Gly
ENST00000305242.9:c.1237C>G ENSP00000306410.5:p.Arg413Gly
ENST00000434029.1:c.919C>G ENSP00000398155.1:p.Arg307Gly
ENST00000480504.1:n.494C>G
ENST00000672841.1:c.313C>G ENSP00000499983.1:p.Arg105Gly
ENST00000672877.1:c.-187-7209C>G ENSP00000500120.1:n.-187-7209C>G
ENST00000673384.1:c.313C>G ENSP00000500856.1:p.Arg105Gly
ENST00000673439.1:c.1237C>G ENSP00000500782.1:p.Arg413Gly
XM_011519526.1:c.1237C>G XP_011517828.1:p.Arg413Gly
XM_011519527.1:c.1237C>G XP_011517829.1:p.Arg413Gly
XM_011519528.1:c.1237C>G XP_011517830.1:p.Arg413Gly
XM_011519529.1:c.1237C>G XP_011517831.1:p.Arg413Gly
XM_011519530.1:c.1237C>G XP_011517832.1:p.Arg413Gly
XM_011519531.1:c.1237C>G XP_011517833.1:p.Arg413Gly
XM_011519532.1:c.1237C>G XP_011517834.1:p.Arg413Gly
XM_011519533.1:c.313C>G XP_011517835.1:p.Arg105Gly
XM_011519534.1:c.313C>G XP_011517836.1:p.Arg105Gly
XM_011519535.1:c.151C>G XP_011517837.1:p.Arg51Gly
XM_011519536.1:c.1237C>G XP_011517838.1:p.Arg413Gly
XM_017016371.1:c.1237C>G XP_016871860.1:p.Arg413Gly
XM_024448049.1:c.1237C>G XP_024303817.1:p.Arg413Gly
XM_024448050.1:c.1237C>G XP_024303818.1:p.Arg413Gly
XM_024448051.1:c.1237C>G XP_024303819.1:p.Arg413Gly
XM_024448052.1:c.1237C>G XP_024303820.1:p.Arg413Gly
XM_024448053.1:c.1237C>G XP_024303821.1:p.Arg413Gly
XM_024448054.1:c.1237C>G XP_024303822.1:p.Arg413Gly
XM_024448055.1:c.313C>G XP_024303823.1:p.Arg105Gly
XM_024448056.1:c.313C>G XP_024303824.1:p.Arg105Gly
XM_024448057.1:c.151C>G XP_024303825.1:p.Arg51Gly