Canonical Allele Identifier: CA406662106
Community Standard Title: NM_001364171.2(ODAD1):c.742C>T (p.Gln248Ter)
Gene: ODAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48304064G>A , CM000681.2:g.48304064G>A GRCh38
NC_000019.9:g.48807321G>A , CM000681.1:g.48807321G>A GRCh37
NC_000019.8:g.53499133G>A NCBI36
NG_033251.1:g.21012C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001364171.2:c.742C>T MANE Select NP_001351100.1:p.Gln248Ter
ENST00000674294.1:c.742C>T MANE Select ENSP00000501363.1:p.Gln248Ter
NM_001364171.1:c.742C>T NP_001351100.1:p.Gln248Ter
NM_144577.3:c.631C>T NP_653178.3:p.Gln211Ter
NM_144577.4:c.631C>T NP_653178.3:p.Gln211Ter
ENST00000315396.7:c.631C>T ENSP00000318429.7:p.Gln211Ter
ENST00000474199.5:n.759C>T
ENST00000474199.6:c.742C>T ENSP00000501357.1:p.Gln248Ter
ENST00000674207.1:c.*450C>T ENSP00000501374.1:n.*450C>T
XM_005259413.2:c.742C>T XP_005259470.1:p.Gln248Ter
XM_005259414.2:c.742C>T XP_005259471.1:p.Gln248Ter
XM_005259414.3:c.742C>T XP_005259471.1:p.Gln248Ter
XM_005259415.2:c.742C>T XP_005259472.1:p.Gln248Ter
XM_005259415.3:c.742C>T XP_005259472.1:p.Gln248Ter
XM_005259416.3:c.58C>T XP_005259473.1:p.Gln20Ter
XM_005259416.4:c.58C>T XP_005259473.1:p.Gln20Ter
XM_011527515.1:c.631C>T XP_011525817.1:p.Gln211Ter
XM_011527515.2:c.631C>T XP_011525817.1:p.Gln211Ter
XM_011527516.1:c.631C>T XP_011525818.1:p.Gln211Ter
XM_011527516.2:c.631C>T XP_011525818.1:p.Gln211Ter
XM_011527517.1:c.742C>T XP_011525819.1:p.Gln248Ter
XM_011527518.1:c.742C>T XP_011525820.1:p.Gln248Ter
XM_017027483.1:c.466C>T XP_016882972.1:p.Gln156Ter
XM_024451782.1:c.781C>T XP_024307550.1:p.Gln261Ter
XM_024451783.1:c.742C>T XP_024307551.1:p.Gln248Ter