Canonical Allele Identifier: CA2339831781

Gene: ODAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48303953C= , CM000681.2:g.48303953C=	GRCh38
NC_000019.9:g.48807210C= , CM000681.1:g.48807210C=	GRCh37
NC_000019.8:g.53499022C=	NCBI36
NG_033251.1:g.21123G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001364171.2:c.853G= MANE Select	NP_001351100.1:p.Ala285=
ENST00000674294.1:c.853G= MANE Select	ENSP00000501363.1:p.Ala285=
NM_001364171.1:c.853G=	NP_001351100.1:p.Ala285=
NM_144577.3:c.742G=	NP_653178.3:p.Ala248=
NM_144577.4:c.742G=	NP_653178.3:p.Ala248=
ENST00000315396.7:c.742G=	ENSP00000318429.7:p.Ala248=
ENST00000474199.5:n.870G=
ENST00000474199.6:c.853G=	ENSP00000501357.1:p.Ala285=
ENST00000674207.1:c.*561G=	ENSP00000501374.1:n.*561G=
XM_005259413.2:c.853G=	XP_005259470.1:p.Ala285=
XM_005259414.2:c.853G=	XP_005259471.1:p.Ala285=
XM_005259414.3:c.853G=	XP_005259471.1:p.Ala285=
XM_005259415.2:c.853G=	XP_005259472.1:p.Ala285=
XM_005259415.3:c.853G=	XP_005259472.1:p.Ala285=
XM_005259416.3:c.169G=	XP_005259473.1:p.Ala57=
XM_005259416.4:c.169G=	XP_005259473.1:p.Ala57=
XM_011527515.1:c.742G=	XP_011525817.1:p.Ala248=
XM_011527515.2:c.742G=	XP_011525817.1:p.Ala248=
XM_011527516.1:c.742G=	XP_011525818.1:p.Ala248=
XM_011527516.2:c.742G=	XP_011525818.1:p.Ala248=
XM_011527517.1:c.853G=	XP_011525819.1:p.Ala285=
XM_011527518.1:c.853G=	XP_011525820.1:p.Ala285=
XM_017027483.1:c.577G=	XP_016882972.1:p.Ala193=
XM_024451782.1:c.892G=	XP_024307550.1:p.Ala298=
XM_024451783.1:c.853G=	XP_024307551.1:p.Ala285=