Canonical Allele Identifier: CA1344415957

Gene: OXTR CAV3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8767465_8767471delinsGGCCGCC , CM000665.2:g.8767465_8767471delinsGGCCGCC	GRCh38
NC_000003.11:g.8809151_8809157delinsGGCCGCC , CM000665.1:g.8809151_8809157delinsGGCCGCC	GRCh37
NC_000003.10:g.8784151_8784157delinsGGCCGCC	NCBI36
NG_008797.2:g.38656_38662delinsGGCCGCC , LRG_329:g.38656_38662delinsGGCCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316793.8:c.717_723delinsGGCGGCC (OXTR) MANE Select	ENSP00000324270.2:p.Ala239=
ENST00000316793.7:c.717_723delinsGGCGGCC (OXTR)	ENSP00000324270.2:p.Ala239=
ENST00000472766.1:n.156-10012_156-10006delinsGGCCGCC (CAV3)
NM_000916.3:c.717_723delinsGGCGGCC (OXTR)	NP_000907.2:p.Ala239=
XM_011533762.1:c.717_723delinsGGCGGCC (OXTR)	XP_011532064.1:p.Ala239=
XM_011533763.1:c.717_723delinsGGCGGCC (OXTR)	XP_011532065.1:p.Ala239=
NM_001354653.1:c.717_723delinsGGCGGCC (OXTR)	NP_001341582.1:p.Ala239=
NM_001354654.1:c.717_723delinsGGCGGCC (OXTR)	NP_001341583.1:p.Ala239=
NM_001354655.1:c.717_723delinsGGCGGCC (OXTR)	NP_001341584.1:p.Ala239=
NM_001354656.1:c.717_723delinsGGCGGCC (OXTR)	NP_001341585.1:p.Ala239=
NM_001354656.2:c.717_723delinsGGCGGCC (OXTR)	NP_001341585.1:p.Ala239=
NM_000916.4:c.717_723delinsGGCGGCC (OXTR) MANE Select	NP_000907.2:p.Ala239=
NM_001354653.2:c.717_723delinsGGCGGCC (OXTR)	NP_001341582.1:p.Ala239=
NM_001354654.2:c.717_723delinsGGCGGCC (OXTR)	NP_001341583.1:p.Ala239=
NM_001354655.2:c.717_723delinsGGCGGCC (OXTR)	NP_001341584.1:p.Ala239=
NM_001354656.3:c.717_723delinsGGCGGCC (OXTR)	NP_001341585.1:p.Ala239=