Canonical Allele Identifier: CA2339829151
Community Standard Title: NM_001364171.2(ODAD1):c.1423G= (p.Asp475=)
Gene: ODAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48298079C= , CM000681.2:g.48298079C= GRCh38
NC_000019.9:g.48801336C= , CM000681.1:g.48801336C= GRCh37
NC_000019.8:g.53493148C= NCBI36
NG_033251.1:g.26997G=

Transcript Alleles

HGVS Amino-acid Change
NM_001364171.2:c.1423G= MANE Select NP_001351100.1:p.Asp475=
ENST00000674294.1:c.1423G= MANE Select ENSP00000501363.1:p.Asp475=
NM_001364171.1:c.1423G= NP_001351100.1:p.Asp475=
NM_144577.3:c.1312G= NP_653178.3:p.Asp438=
NM_144577.4:c.1312G= NP_653178.3:p.Asp438=
ENST00000315396.7:c.1312G= ENSP00000318429.7:p.Asp438=
ENST00000474199.5:n.1440G=
ENST00000474199.6:c.1423G= ENSP00000501357.1:p.Asp475=
ENST00000497273.1:n.839G=
ENST00000674207.1:c.*1112+98G= ENSP00000501374.1:n.*1112+98G=
XM_005259413.2:c.1423G= XP_005259470.1:p.Asp475=
XM_005259414.2:c.1423G= XP_005259471.1:p.Asp475=
XM_005259414.3:c.1423G= XP_005259471.1:p.Asp475=
XM_005259415.2:c.1423G= XP_005259472.1:p.Asp475=
XM_005259415.3:c.1423G= XP_005259472.1:p.Asp475=
XM_005259416.3:c.739G= XP_005259473.1:p.Asp247=
XM_005259416.4:c.739G= XP_005259473.1:p.Asp247=
XM_011527515.1:c.1312G= XP_011525817.1:p.Asp438=
XM_011527515.2:c.1312G= XP_011525817.1:p.Asp438=
XM_011527516.1:c.1312G= XP_011525818.1:p.Asp438=
XM_011527516.2:c.1312G= XP_011525818.1:p.Asp438=
XM_017027483.1:c.1147G= XP_016882972.1:p.Asp383=
XM_024451782.1:c.1462G= XP_024307550.1:p.Asp488=
XM_024451783.1:c.1423G= XP_024307551.1:p.Asp475=