Canonical Allele Identifier: CA309294790

Gene: ODAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48298076C>T , CM000681.2:g.48298076C>T	GRCh38
NC_000019.9:g.48801333C>T , CM000681.1:g.48801333C>T	GRCh37
NC_000019.8:g.53493145C>T	NCBI36
NG_033251.1:g.27000G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001364171.2:c.1426G>A MANE Select	NP_001351100.1:p.Ala476Thr
ENST00000674294.1:c.1426G>A MANE Select	ENSP00000501363.1:p.Ala476Thr
NM_001364171.1:c.1426G>A	NP_001351100.1:p.Ala476Thr
NM_144577.3:c.1315G>A	NP_653178.3:p.Ala439Thr
NM_144577.4:c.1315G>A	NP_653178.3:p.Ala439Thr
ENST00000315396.7:c.1315G>A	ENSP00000318429.7:p.Ala439Thr
ENST00000474199.5:n.1443G>A
ENST00000474199.6:c.1426G>A	ENSP00000501357.1:p.Ala476Thr
ENST00000497273.1:n.842G>A
ENST00000674207.1:c.*1112+101G>A	ENSP00000501374.1:n.*1112+101G>A
XM_005259413.2:c.1426G>A	XP_005259470.1:p.Ala476Thr
XM_005259414.2:c.1426G>A	XP_005259471.1:p.Ala476Thr
XM_005259414.3:c.1426G>A	XP_005259471.1:p.Ala476Thr
XM_005259415.2:c.1426G>A	XP_005259472.1:p.Ala476Thr
XM_005259415.3:c.1426G>A	XP_005259472.1:p.Ala476Thr
XM_005259416.3:c.742G>A	XP_005259473.1:p.Ala248Thr
XM_005259416.4:c.742G>A	XP_005259473.1:p.Ala248Thr
XM_011527515.1:c.1315G>A	XP_011525817.1:p.Ala439Thr
XM_011527515.2:c.1315G>A	XP_011525817.1:p.Ala439Thr
XM_011527516.1:c.1315G>A	XP_011525818.1:p.Ala439Thr
XM_011527516.2:c.1315G>A	XP_011525818.1:p.Ala439Thr
XM_017027483.1:c.1150G>A	XP_016882972.1:p.Ala384Thr
XM_024451782.1:c.1465G>A	XP_024307550.1:p.Ala489Thr
XM_024451783.1:c.1426G>A	XP_024307551.1:p.Ala476Thr