Canonical Allele Identifier: CA9548979

Gene: ODAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48304099G>A , CM000681.2:g.48304099G>A	GRCh38
NC_000019.9:g.48807356G>A , CM000681.1:g.48807356G>A	GRCh37
NC_000019.8:g.53499168G>A	NCBI36
NG_033251.1:g.20977C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001364171.2:c.707C>T MANE Select	NP_001351100.1:p.Ala236Val
ENST00000674294.1:c.707C>T MANE Select	ENSP00000501363.1:p.Ala236Val
NM_001364171.1:c.707C>T	NP_001351100.1:p.Ala236Val
NM_144577.3:c.596C>T	NP_653178.3:p.Ala199Val
NM_144577.4:c.596C>T	NP_653178.3:p.Ala199Val
ENST00000315396.7:c.596C>T	ENSP00000318429.7:p.Ala199Val
ENST00000474199.5:n.724C>T
ENST00000474199.6:c.707C>T	ENSP00000501357.1:p.Ala236Val
ENST00000674207.1:c.*415C>T	ENSP00000501374.1:n.*415C>T
XM_005259413.2:c.707C>T	XP_005259470.1:p.Ala236Val
XM_005259414.2:c.707C>T	XP_005259471.1:p.Ala236Val
XM_005259414.3:c.707C>T	XP_005259471.1:p.Ala236Val
XM_005259415.2:c.707C>T	XP_005259472.1:p.Ala236Val
XM_005259415.3:c.707C>T	XP_005259472.1:p.Ala236Val
XM_005259416.3:c.23C>T	XP_005259473.1:p.Ala8Val
XM_005259416.4:c.23C>T	XP_005259473.1:p.Ala8Val
XM_011527515.1:c.596C>T	XP_011525817.1:p.Ala199Val
XM_011527515.2:c.596C>T	XP_011525817.1:p.Ala199Val
XM_011527516.1:c.596C>T	XP_011525818.1:p.Ala199Val
XM_011527516.2:c.596C>T	XP_011525818.1:p.Ala199Val
XM_011527517.1:c.707C>T	XP_011525819.1:p.Ala236Val
XM_011527518.1:c.707C>T	XP_011525820.1:p.Ala236Val
XM_017027483.1:c.431C>T	XP_016882972.1:p.Ala144Val
XM_024451782.1:c.746C>T	XP_024307550.1:p.Ala249Val
XM_024451783.1:c.707C>T	XP_024307551.1:p.Ala236Val