Canonical Allele Identifier: CA376391812
Gene: ODAD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27936766C>G , CM000672.2:g.27936766C>G GRCh38
NC_000010.10:g.28225695C>G , CM000672.1:g.28225695C>G GRCh37
NC_000010.9:g.28265701C>G NCBI36
NG_042820.1:g.67285G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305242.10:c.2212G>C MANE Select ENSP00000306410.5:p.Ala738Pro
ENST00000672841.1:c.1288G>C ENSP00000499983.1:p.Ala430Pro
ENST00000672877.1:c.787G>C ENSP00000500120.1:p.Ala263Pro
ENST00000673384.1:c.1288G>C ENSP00000500856.1:p.Ala430Pro
ENST00000673439.1:c.2212G>C ENSP00000500782.1:p.Ala738Pro
ENST00000305242.9:c.2212G>C ENSP00000306410.5:p.Ala738Pro
NM_001290020.1:c.2212G>C NP_001276949.1:p.Ala738Pro
NM_001290021.1:c.787G>C NP_001276950.1:p.Ala263Pro
NM_001312689.1:c.1288G>C NP_001299618.1:p.Ala430Pro
NM_018076.3:c.2212G>C NP_060546.2:p.Ala738Pro
NM_018076.4:c.2212G>C NP_060546.2:p.Ala738Pro
XM_011519526.1:c.2212G>C XP_011517828.1:p.Ala738Pro
XM_011519527.1:c.2212G>C XP_011517829.1:p.Ala738Pro
XM_011519528.1:c.2212G>C XP_011517830.1:p.Ala738Pro
XM_011519529.1:c.2212G>C XP_011517831.1:p.Ala738Pro
XM_011519530.1:c.2212G>C XP_011517832.1:p.Ala738Pro
XM_011519531.1:c.2212G>C XP_011517833.1:p.Ala738Pro
XM_011519532.1:c.2002G>C XP_011517834.1:p.Ala668Pro
XM_011519533.1:c.1288G>C XP_011517835.1:p.Ala430Pro
XM_011519534.1:c.1288G>C XP_011517836.1:p.Ala430Pro
XM_011519535.1:c.1126G>C XP_011517837.1:p.Ala376Pro
XM_011519537.1:c.787G>C XP_011517839.1:p.Ala263Pro
XM_024448049.1:c.2212G>C XP_024303817.1:p.Ala738Pro
XM_024448050.1:c.2212G>C XP_024303818.1:p.Ala738Pro
XM_024448051.1:c.2212G>C XP_024303819.1:p.Ala738Pro
XM_024448052.1:c.2212G>C XP_024303820.1:p.Ala738Pro
XM_024448053.1:c.2212G>C XP_024303821.1:p.Ala738Pro
XM_024448054.1:c.2002G>C XP_024303822.1:p.Ala668Pro
XM_024448055.1:c.1288G>C XP_024303823.1:p.Ala430Pro
XM_024448056.1:c.1288G>C XP_024303824.1:p.Ala430Pro
XM_024448057.1:c.1126G>C XP_024303825.1:p.Ala376Pro
XM_024448058.1:c.787G>C XP_024303826.1:p.Ala263Pro
NM_001290020.2:c.2212G>C NP_001276949.1:p.Ala738Pro
NM_001290021.2:c.787G>C NP_001276950.1:p.Ala263Pro
NM_001312689.2:c.1288G>C NP_001299618.1:p.Ala430Pro
NM_018076.5:c.2212G>C MANE Select NP_060546.2:p.Ala738Pro