Canonical Allele Identifier: CA5453641
Community Standard Title: NM_018076.5(ODAD2):c.1076G>A (p.Trp359Ter)
Gene: ODAD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27971174C>T , CM000672.2:g.27971174C>T GRCh38
NC_000010.10:g.28260103C>T , CM000672.1:g.28260103C>T GRCh37
NC_000010.9:g.28300109C>T NCBI36
NG_042820.1:g.32877G>A

Transcript Alleles

HGVS Amino-acid Change
NM_018076.5:c.1076G>A MANE Select NP_060546.2:p.Trp359Ter
ENST00000305242.10:c.1076G>A MANE Select ENSP00000306410.5:p.Trp359Ter
NM_001290020.1:c.1076G>A NP_001276949.1:p.Trp359Ter
NM_001290020.2:c.1076G>A NP_001276949.1:p.Trp359Ter
NM_001290021.1:c.-187-9459G>A NP_001276950.1:n.-187-9459G>A
NM_001290021.2:c.-187-9459G>A NP_001276950.1:n.-187-9459G>A
NM_001312689.1:c.152G>A NP_001299618.1:p.Trp51Ter
NM_001312689.2:c.152G>A NP_001299618.1:p.Trp51Ter
NM_018076.3:c.1076G>A NP_060546.2:p.Trp359Ter
NM_018076.4:c.1076G>A NP_060546.2:p.Trp359Ter
ENST00000305242.9:c.1076G>A ENSP00000306410.5:p.Trp359Ter
ENST00000434029.1:c.758G>A ENSP00000398155.1:p.Trp253Ter
ENST00000480504.1:n.333G>A
ENST00000672841.1:c.152G>A ENSP00000499983.1:p.Trp51Ter
ENST00000672877.1:c.-187-9459G>A ENSP00000500120.1:n.-187-9459G>A
ENST00000673384.1:c.152G>A ENSP00000500856.1:p.Trp51Ter
ENST00000673439.1:c.1076G>A ENSP00000500782.1:p.Trp359Ter
ENST00000673512.1:c.152G>A ENSP00000499923.1:p.Trp51Ter
XM_011519526.1:c.1076G>A XP_011517828.1:p.Trp359Ter
XM_011519527.1:c.1076G>A XP_011517829.1:p.Trp359Ter
XM_011519528.1:c.1076G>A XP_011517830.1:p.Trp359Ter
XM_011519529.1:c.1076G>A XP_011517831.1:p.Trp359Ter
XM_011519530.1:c.1076G>A XP_011517832.1:p.Trp359Ter
XM_011519531.1:c.1076G>A XP_011517833.1:p.Trp359Ter
XM_011519532.1:c.1076G>A XP_011517834.1:p.Trp359Ter
XM_011519533.1:c.152G>A XP_011517835.1:p.Trp51Ter
XM_011519534.1:c.152G>A XP_011517836.1:p.Trp51Ter
XM_011519535.1:c.-11G>A XP_011517837.1:n.-11G>A
XM_011519536.1:c.1076G>A XP_011517838.1:p.Trp359Ter
XM_017016371.1:c.1076G>A XP_016871860.1:p.Trp359Ter
XM_024448049.1:c.1076G>A XP_024303817.1:p.Trp359Ter
XM_024448050.1:c.1076G>A XP_024303818.1:p.Trp359Ter
XM_024448051.1:c.1076G>A XP_024303819.1:p.Trp359Ter
XM_024448052.1:c.1076G>A XP_024303820.1:p.Trp359Ter
XM_024448053.1:c.1076G>A XP_024303821.1:p.Trp359Ter
XM_024448054.1:c.1076G>A XP_024303822.1:p.Trp359Ter
XM_024448055.1:c.152G>A XP_024303823.1:p.Trp51Ter
XM_024448056.1:c.152G>A XP_024303824.1:p.Trp51Ter
XM_024448057.1:c.-11G>A XP_024303825.1:n.-11G>A