Canonical Allele Identifier: CA5453117
Gene: ODAD2 HGNC NCBI

Linked Data

dbSNP Id: rs763367784

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27862464_27862466del , CM000672.2:g.27862464_27862466del GRCh38
NC_000010.10:g.28151393_28151395del , CM000672.1:g.28151393_28151395del GRCh37
NC_000010.9:g.28191399_28191401del NCBI36
NG_042820.1:g.141588_141590del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305242.10:c.2770_2772del MANE Select ENSP00000306410.5:p.Val924del
ENST00000672841.1:c.1846_1848del ENSP00000499983.1:p.Val616del
ENST00000672877.1:c.1345_1347del ENSP00000500120.1:p.Val449del
ENST00000673384.1:c.1846_1848del ENSP00000500856.1:p.Val616del
ENST00000673439.1:c.2770_2772del ENSP00000500782.1:p.Val924del
ENST00000305242.9:c.2770_2772del ENSP00000306410.5:p.Val924del
NM_001290020.1:c.2770_2772del NP_001276949.1:p.Val924del
NM_001290021.1:c.1345_1347del NP_001276950.1:p.Val449del
NM_001312689.1:c.1846_1848del NP_001299618.1:p.Val616del
NM_018076.3:c.2770_2772del NP_060546.2:p.Val924del
NM_018076.4:c.2770_2772del NP_060546.2:p.Val924del
XM_011519526.1:c.2770_2772del XP_011517828.1:p.Val924del
XM_011519527.1:c.2770_2772del XP_011517829.1:p.Val924del
XM_011519528.1:c.2770_2772del XP_011517830.1:p.Val924del
XM_011519529.1:c.2770_2772del XP_011517831.1:p.Val924del
XM_011519530.1:c.2770_2772del XP_011517832.1:p.Val924del
XM_011519531.1:c.2770_2772del XP_011517833.1:p.Val924del
XM_011519532.1:c.2560_2562del XP_011517834.1:p.Val854del
XM_011519533.1:c.1846_1848del XP_011517835.1:p.Val616del
XM_011519534.1:c.1846_1848del XP_011517836.1:p.Val616del
XM_011519535.1:c.1684_1686del XP_011517837.1:p.Val562del
XM_011519537.1:c.1345_1347del XP_011517839.1:p.Val449del
XM_024448049.1:c.2899_2901del XP_024303817.1:p.Val967del
XM_024448050.1:c.2899_2901del XP_024303818.1:p.Val967del
XM_024448051.1:c.2899_2901del XP_024303819.1:p.Val967del
XM_024448052.1:c.2899_2901del XP_024303820.1:p.Val967del
XM_024448053.1:c.2899_2901del XP_024303821.1:p.Val967del
XM_024448054.1:c.2689_2691del XP_024303822.1:p.Val897del
XM_024448055.1:c.1975_1977del XP_024303823.1:p.Val659del
XM_024448056.1:c.1975_1977del XP_024303824.1:p.Val659del
XM_024448057.1:c.1813_1815del XP_024303825.1:p.Val605del
XM_024448058.1:c.1474_1476del XP_024303826.1:p.Val492del
NM_001290020.2:c.2770_2772del NP_001276949.1:p.Val924del
NM_001290021.2:c.1345_1347del NP_001276950.1:p.Val449del
NM_001312689.2:c.1846_1848del NP_001299618.1:p.Val616del
NM_018076.5:c.2770_2772del MANE Select NP_060546.2:p.Val924del