Canonical Allele Identifier: CA2339831864

Gene: ODAD1

Linked Data

• ClinVar Variation Id: 1040706
• ClinVar RCV Id: RCV001344393
• dbSNP Id: rs1968544779

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48304109_48304110delinsAA , CM000681.2:g.48304109_48304110delinsAA	GRCh38
NC_000019.9:g.48807366_48807367delinsAA , CM000681.1:g.48807366_48807367delinsAA	GRCh37
NC_000019.8:g.53499178_53499179delinsAA	NCBI36
NG_033251.1:g.20966_20967delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474199.6:c.696_697delinsTT	ENSP00000501357.1:p.Arg233Trp
ENST00000674207.1:c.*404_*405delinsTT	ENSP00000501374.1:n.*404_*405delinsTT
ENST00000674294.1:c.696_697delinsTT MANE Select	ENSP00000501363.1:p.Arg233Trp
ENST00000315396.7:c.585_586delinsTT	ENSP00000318429.7:p.Arg196Trp
ENST00000474199.5:n.713_714delinsTT
NM_144577.3:c.585_586delinsTT	NP_653178.3:p.Arg196Trp
XM_005259413.2:c.696_697delinsTT	XP_005259470.1:p.Arg233Trp
XM_005259414.2:c.696_697delinsTT	XP_005259471.1:p.Arg233Trp
XM_005259415.2:c.696_697delinsTT	XP_005259472.1:p.Arg233Trp
XM_005259416.3:c.12_13delinsTT	XP_005259473.1:p.Arg5Trp
XM_011527515.1:c.585_586delinsTT	XP_011525817.1:p.Arg196Trp
XM_011527516.1:c.585_586delinsTT	XP_011525818.1:p.Arg196Trp
XM_011527517.1:c.696_697delinsTT	XP_011525819.1:p.Arg233Trp
XM_011527518.1:c.696_697delinsTT	XP_011525820.1:p.Arg233Trp
NM_001364171.1:c.696_697delinsTT	NP_001351100.1:p.Arg233Trp
NM_144577.4:c.585_586delinsTT	NP_653178.3:p.Arg196Trp
XM_005259414.3:c.696_697delinsTT	XP_005259471.1:p.Arg233Trp
XM_005259415.3:c.696_697delinsTT	XP_005259472.1:p.Arg233Trp
XM_005259416.4:c.12_13delinsTT	XP_005259473.1:p.Arg5Trp
XM_011527515.2:c.585_586delinsTT	XP_011525817.1:p.Arg196Trp
XM_011527516.2:c.585_586delinsTT	XP_011525818.1:p.Arg196Trp
XM_017027483.1:c.420_421delinsTT	XP_016882972.1:p.Arg141Trp
XM_024451782.1:c.735_736delinsTT	XP_024307550.1:p.Arg246Trp
XM_024451783.1:c.696_697delinsTT	XP_024307551.1:p.Arg233Trp
NM_001364171.2:c.696_697delinsTT MANE Select	NP_001351100.1:p.Arg233Trp