Canonical Allele Identifier: CA508263416

Gene: ODAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48318489G>A , CM000681.2:g.48318489G>A	GRCh38
NC_000019.9:g.48821746G>A , CM000681.1:g.48821746G>A	GRCh37
NC_000019.8:g.53513558G>A	NCBI36
NG_033251.1:g.6587C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001364171.2:c.258C>T MANE Select	NP_001351100.1:p.Asp86=
ENST00000674294.1:c.258C>T MANE Select	ENSP00000501363.1:p.Asp86=
NM_001364171.1:c.258C>T	NP_001351100.1:p.Asp86=
NM_144577.3:c.147C>T	NP_653178.3:p.Asp49=
NM_144577.4:c.147C>T	NP_653178.3:p.Asp49=
ENST00000315396.7:c.147C>T	ENSP00000318429.7:p.Asp49=
ENST00000474199.5:n.275C>T
ENST00000474199.6:c.258C>T	ENSP00000501357.1:p.Asp86=
ENST00000497803.1:n.534C>T
ENST00000504608.6:n.324+1810C>T
ENST00000674207.1:c.158C>T	ENSP00000501374.1:p.Thr53Ile
ENST00000674234.1:n.324+1810C>T
XM_005259413.2:c.258C>T	XP_005259470.1:p.Asp86=
XM_005259414.2:c.258C>T	XP_005259471.1:p.Asp86=
XM_005259414.3:c.258C>T	XP_005259471.1:p.Asp86=
XM_005259415.2:c.258C>T	XP_005259472.1:p.Asp86=
XM_005259415.3:c.258C>T	XP_005259472.1:p.Asp86=
XM_011527515.1:c.147C>T	XP_011525817.1:p.Asp49=
XM_011527515.2:c.147C>T	XP_011525817.1:p.Asp49=
XM_011527516.1:c.147C>T	XP_011525818.1:p.Asp49=
XM_011527516.2:c.147C>T	XP_011525818.1:p.Asp49=
XM_011527517.1:c.258C>T	XP_011525819.1:p.Asp86=
XM_011527518.1:c.258C>T	XP_011525820.1:p.Asp86=
XM_017027483.1:c.-19C>T	XP_016882972.1:n.-19C>T
XM_024451782.1:c.297C>T	XP_024307550.1:p.Asp99=
XM_024451783.1:c.258C>T	XP_024307551.1:p.Asp86=