Canonical Allele Identifier: CA10603120
Community Standard Title: NM_018076.5(ODAD2):c.2406del (p.Val803Ter)
Gene: ODAD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27935100del , CM000672.2:g.27935100del GRCh38
NC_000010.10:g.28224029del , CM000672.1:g.28224029del GRCh37
NC_000010.9:g.28264035del NCBI36
NG_042820.1:g.68952del

Transcript Alleles

HGVS Amino-acid Change
NM_018076.5:c.2406del MANE Select NP_060546.2:p.Val803Ter
ENST00000305242.10:c.2406del MANE Select ENSP00000306410.5:p.Val803Ter
NM_001290020.1:c.2406del NP_001276949.1:p.Val803Ter
NM_001290020.2:c.2406del NP_001276949.1:p.Val803Ter
NM_001290021.1:c.981del NP_001276950.1:p.Val328Ter
NM_001290021.2:c.981del NP_001276950.1:p.Val328Ter
NM_001312689.1:c.1482del NP_001299618.1:p.Val495Ter
NM_001312689.2:c.1482del NP_001299618.1:p.Val495Ter
NM_018076.3:c.2406del NP_060546.2:p.Val803Ter
NM_018076.4:c.2406del NP_060546.2:p.Val803Ter
ENST00000305242.9:c.2406del ENSP00000306410.5:p.Val803Ter
ENST00000672841.1:c.1482del ENSP00000499983.1:p.Val495Ter
ENST00000672877.1:c.981del ENSP00000500120.1:p.Val328Ter
ENST00000673384.1:c.1482del ENSP00000500856.1:p.Val495Ter
ENST00000673439.1:c.2406del ENSP00000500782.1:p.Val803Ter
XM_011519526.1:c.2406del XP_011517828.1:p.Val803Ter
XM_011519527.1:c.2406del XP_011517829.1:p.Val803Ter
XM_011519528.1:c.2406del XP_011517830.1:p.Val803Ter
XM_011519529.1:c.2406del XP_011517831.1:p.Val803Ter
XM_011519530.1:c.2406del XP_011517832.1:p.Val803Ter
XM_011519531.1:c.2406del XP_011517833.1:p.Val803Ter
XM_011519532.1:c.2196del XP_011517834.1:p.Val733Ter
XM_011519533.1:c.1482del XP_011517835.1:p.Val495Ter
XM_011519534.1:c.1482del XP_011517836.1:p.Val495Ter
XM_011519535.1:c.1320del XP_011517837.1:p.Val441Ter
XM_011519537.1:c.981del XP_011517839.1:p.Val328Ter
XM_024448049.1:c.2406del XP_024303817.1:p.Val803Ter
XM_024448050.1:c.2406del XP_024303818.1:p.Val803Ter
XM_024448051.1:c.2406del XP_024303819.1:p.Val803Ter
XM_024448052.1:c.2406del XP_024303820.1:p.Val803Ter
XM_024448053.1:c.2406del XP_024303821.1:p.Val803Ter
XM_024448054.1:c.2196del XP_024303822.1:p.Val733Ter
XM_024448055.1:c.1482del XP_024303823.1:p.Val495Ter
XM_024448056.1:c.1482del XP_024303824.1:p.Val495Ter
XM_024448057.1:c.1320del XP_024303825.1:p.Val441Ter
XM_024448058.1:c.981del XP_024303826.1:p.Val328Ter