Canonical Allele Identifier: CA376397609
Community Standard Title: NM_018076.5(ODAD2):c.316C>T (p.Gln106Ter)
Gene: ODAD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27987452G>A , CM000672.2:g.27987452G>A GRCh38
NC_000010.10:g.28276381G>A , CM000672.1:g.28276381G>A GRCh37
NC_000010.9:g.28316387G>A NCBI36
NG_042820.1:g.16599C>T

Transcript Alleles

HGVS Amino-acid Change
NM_018076.5:c.316C>T MANE Select NP_060546.2:p.Gln106Ter
ENST00000305242.10:c.316C>T MANE Select ENSP00000306410.5:p.Gln106Ter
NM_001290020.1:c.316C>T NP_001276949.1:p.Gln106Ter
NM_001290020.2:c.316C>T NP_001276949.1:p.Gln106Ter
NM_018076.3:c.316C>T NP_060546.2:p.Gln106Ter
NM_018076.4:c.316C>T NP_060546.2:p.Gln106Ter
ENST00000305242.9:c.316C>T ENSP00000306410.5:p.Gln106Ter
ENST00000673439.1:c.316C>T ENSP00000500782.1:p.Gln106Ter
XM_011519526.1:c.316C>T XP_011517828.1:p.Gln106Ter
XM_011519527.1:c.316C>T XP_011517829.1:p.Gln106Ter
XM_011519528.1:c.316C>T XP_011517830.1:p.Gln106Ter
XM_011519529.1:c.316C>T XP_011517831.1:p.Gln106Ter
XM_011519530.1:c.316C>T XP_011517832.1:p.Gln106Ter
XM_011519531.1:c.316C>T XP_011517833.1:p.Gln106Ter
XM_011519532.1:c.316C>T XP_011517834.1:p.Gln106Ter
XM_011519536.1:c.316C>T XP_011517838.1:p.Gln106Ter
XM_017016371.1:c.316C>T XP_016871860.1:p.Gln106Ter
XM_024448049.1:c.316C>T XP_024303817.1:p.Gln106Ter
XM_024448050.1:c.316C>T XP_024303818.1:p.Gln106Ter
XM_024448051.1:c.316C>T XP_024303819.1:p.Gln106Ter
XM_024448052.1:c.316C>T XP_024303820.1:p.Gln106Ter
XM_024448053.1:c.316C>T XP_024303821.1:p.Gln106Ter
XM_024448054.1:c.316C>T XP_024303822.1:p.Gln106Ter
XR_002957065.1:n.86+4171G>A