Canonical Allele Identifier: CA1344413732

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8762759_8762765delinsTCCTGTG , CM000665.2:g.8762759_8762765delinsTCCTGTG GRCh38
NC_000003.11:g.8804445_8804451delinsTCCTGTG , CM000665.1:g.8804445_8804451delinsTCCTGTG GRCh37
NC_000003.10:g.8779445_8779451delinsTCCTGTG NCBI36
NG_008797.2:g.33950_33956delinsTCCTGTG , LRG_329:g.33950_33956delinsTCCTGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.922+4501_922+4507delinsCACAGGA (OXTR) MANE Select ENSP00000324270.2:n.922+4501_922+4507deli...
ENST00000316793.7:c.922+4501_922+4507delinsCACAGGA (OXTR) ENSP00000324270.2:n.922+4501_922+4507deli...
ENST00000472766.1:n.156-14718_156-14712delinsTCCTGTG (CAV3)
NM_000916.3:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_000907.2:n.922+4501_922+4507delinsCACA...
XM_011533762.1:c.922+4501_922+4507delinsCACAGGA (OXTR) XP_011532064.1:n.922+4501_922+4507delinsC...
XM_011533763.1:c.922+4501_922+4507delinsCACAGGA (OXTR) XP_011532065.1:n.922+4501_922+4507delinsC...
NM_001354653.1:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341582.1:n.922+4501_922+4507delinsC...
NM_001354654.1:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341583.1:n.922+4501_922+4507delinsC...
NM_001354655.1:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341584.1:n.922+4501_922+4507delinsC...
NM_001354656.1:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341585.1:n.922+4501_922+4507delinsC...
NM_001354656.2:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341585.1:n.922+4501_922+4507delinsC...
NM_000916.4:c.922+4501_922+4507delinsCACAGGA (OXTR) MANE Select NP_000907.2:n.922+4501_922+4507delinsCACA...
NM_001354653.2:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341582.1:n.922+4501_922+4507delinsC...
NM_001354654.2:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341583.1:n.922+4501_922+4507delinsC...
NM_001354655.2:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341584.1:n.922+4501_922+4507delinsC...
NM_001354656.3:c.922+4501_922+4507delinsCACAGGA (OXTR) NP_001341585.1:n.922+4501_922+4507delinsC...