Canonical Allele Identifier: CA1344412516

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8760928G= , CM000665.2:g.8760928G= GRCh38
NC_000003.11:g.8802614G= , CM000665.1:g.8802614G= GRCh37
NC_000003.10:g.8777614G= NCBI36
NG_008797.2:g.32119G= , LRG_329:g.32119G=

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.922+6338C= (OXTR) MANE Select ENSP00000324270.2:n.922+6338C=
ENST00000316793.7:c.922+6338C= (OXTR) ENSP00000324270.2:n.922+6338C=
ENST00000472766.1:n.156-16549G= (CAV3)
NM_000916.3:c.922+6338C= (OXTR) NP_000907.2:n.922+6338C=
XM_011533762.1:c.922+6338C= (OXTR) XP_011532064.1:n.922+6338C=
XM_011533763.1:c.922+6338C= (OXTR) XP_011532065.1:n.922+6338C=
NM_001354653.1:c.922+6338C= (OXTR) NP_001341582.1:n.922+6338C=
NM_001354654.1:c.922+6338C= (OXTR) NP_001341583.1:n.922+6338C=
NM_001354655.1:c.922+6338C= (OXTR) NP_001341584.1:n.922+6338C=
NM_001354656.1:c.922+6338C= (OXTR) NP_001341585.1:n.922+6338C=
NM_001354656.2:c.922+6338C= (OXTR) NP_001341585.1:n.922+6338C=
NM_000916.4:c.922+6338C= (OXTR) MANE Select NP_000907.2:n.922+6338C=
NM_001354653.2:c.922+6338C= (OXTR) NP_001341582.1:n.922+6338C=
NM_001354654.2:c.922+6338C= (OXTR) NP_001341583.1:n.922+6338C=
NM_001354655.2:c.922+6338C= (OXTR) NP_001341584.1:n.922+6338C=
NM_001354656.3:c.922+6338C= (OXTR) NP_001341585.1:n.922+6338C=