Canonical Allele Identifier: CA2664272687

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8767308_8767310del , CM000665.2:g.8767308_8767310del GRCh38
NC_000003.11:g.8808994_8808996del , CM000665.1:g.8808994_8808996del GRCh37
NC_000003.10:g.8783994_8783996del NCBI36
NG_008797.2:g.38499_38501del , LRG_329:g.38499_38501del

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.879_881del (OXTR) MANE Select ENSP00000324270.2:p.Phe293_Val294delinsLe...
ENST00000316793.7:c.879_881del (OXTR) ENSP00000324270.2:p.Phe293_Val294delinsLe...
ENST00000472766.1:n.156-10169_156-10167del (CAV3)
NM_000916.3:c.879_881del (OXTR) NP_000907.2:p.Phe293_Val294delinsLeu
XM_011533762.1:c.879_881del (OXTR) XP_011532064.1:p.Phe293_Val294delinsLeu
XM_011533763.1:c.879_881del (OXTR) XP_011532065.1:p.Phe293_Val294delinsLeu
NM_001354653.1:c.879_881del (OXTR) NP_001341582.1:p.Phe293_Val294delinsLeu
NM_001354654.1:c.879_881del (OXTR) NP_001341583.1:p.Phe293_Val294delinsLeu
NM_001354655.1:c.879_881del (OXTR) NP_001341584.1:p.Phe293_Val294delinsLeu
NM_001354656.1:c.879_881del (OXTR) NP_001341585.1:p.Phe293_Val294delinsLeu
NM_001354656.2:c.879_881del (OXTR) NP_001341585.1:p.Phe293_Val294delinsLeu
NM_000916.4:c.879_881del (OXTR) MANE Select NP_000907.2:p.Phe293_Val294delinsLeu
NM_001354653.2:c.879_881del (OXTR) NP_001341582.1:p.Phe293_Val294delinsLeu
NM_001354654.2:c.879_881del (OXTR) NP_001341583.1:p.Phe293_Val294delinsLeu
NM_001354655.2:c.879_881del (OXTR) NP_001341584.1:p.Phe293_Val294delinsLeu
NM_001354656.3:c.879_881del (OXTR) NP_001341585.1:p.Phe293_Val294delinsLeu