Canonical Allele Identifier: CA2735475116

Gene: ODAD3

Linked Data

• dbSNP Id: rs2144755313

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422604_11422605insAGG , CM000681.2:g.11422604_11422605insAGG	GRCh38
NC_000019.9:g.11533272_11533273insAGG , CM000681.1:g.11533272_11533273insAGG	GRCh37
NC_000019.8:g.11394272_11394273insAGG	NCBI36
NG_041777.1:g.18179_18180insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1301_1302insCTC MANE Select	ENSP00000348757.3:p.Ala434_Gln435insSer
ENST00000356392.8:c.1301_1302insCTC	ENSP00000348757.3:p.Ala434_Gln435insSer
ENST00000586836.5:c.728_729insCTC	ENSP00000467429.1:p.Ala243_Gln244insSer
ENST00000591179.5:c.1121_1122insCTC	ENSP00000466800.1:p.Ala374_Gln375insSer
ENST00000591345.5:c.*1220_*1221insCTC	ENSP00000467313.1:n.*1220_*1221insCTC
NM_001302453.1:c.1139_1140insCTC	NP_001289382.1:p.Ala380_Gln381insSer
NM_001302454.1:c.1121_1122insCTC	NP_001289383.1:p.Ala374_Gln375insSer
NM_145045.4:c.1301_1302insCTC	NP_659482.3:p.Ala434_Gln435insSer
NM_145045.5:c.1301_1302insCTC MANE Select	NP_659482.3:p.Ala434_Gln435insSer
NM_001302454.2:c.1121_1122insCTC	NP_001289383.1:p.Ala374_Gln375insSer