Canonical Allele Identifier: CA1344415711

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8766936_8766939delinsTCCA , CM000665.2:g.8766936_8766939delinsTCCA GRCh38
NC_000003.11:g.8808622_8808625delinsTCCA , CM000665.1:g.8808622_8808625delinsTCCA GRCh37
NC_000003.10:g.8783622_8783625delinsTCCA NCBI36
NG_008797.2:g.38127_38130delinsTCCA , LRG_329:g.38127_38130delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.922+327_922+330delinsTGGA (OXTR) MANE Select ENSP00000324270.2:n.922+327_922+330delinsTGGA
ENST00000316793.7:c.922+327_922+330delinsTGGA (OXTR) ENSP00000324270.2:n.922+327_922+330delinsTGGA
ENST00000472766.1:n.156-10541_156-10538delinsTCCA (CAV3)
NM_000916.3:c.922+327_922+330delinsTGGA (OXTR) NP_000907.2:n.922+327_922+330delinsTGGA
XM_011533762.1:c.922+327_922+330delinsTGGA (OXTR) XP_011532064.1:n.922+327_922+330delinsTGGA
XM_011533763.1:c.922+327_922+330delinsTGGA (OXTR) XP_011532065.1:n.922+327_922+330delinsTGGA
NM_001354653.1:c.922+327_922+330delinsTGGA (OXTR) NP_001341582.1:n.922+327_922+330delinsTGGA
NM_001354654.1:c.922+327_922+330delinsTGGA (OXTR) NP_001341583.1:n.922+327_922+330delinsTGGA
NM_001354655.1:c.922+327_922+330delinsTGGA (OXTR) NP_001341584.1:n.922+327_922+330delinsTGGA
NM_001354656.1:c.922+327_922+330delinsTGGA (OXTR) NP_001341585.1:n.922+327_922+330delinsTGGA
NM_001354656.2:c.922+327_922+330delinsTGGA (OXTR) NP_001341585.1:n.922+327_922+330delinsTGGA
NM_000916.4:c.922+327_922+330delinsTGGA (OXTR) MANE Select NP_000907.2:n.922+327_922+330delinsTGGA
NM_001354653.2:c.922+327_922+330delinsTGGA (OXTR) NP_001341582.1:n.922+327_922+330delinsTGGA
NM_001354654.2:c.922+327_922+330delinsTGGA (OXTR) NP_001341583.1:n.922+327_922+330delinsTGGA
NM_001354655.2:c.922+327_922+330delinsTGGA (OXTR) NP_001341584.1:n.922+327_922+330delinsTGGA
NM_001354656.3:c.922+327_922+330delinsTGGA (OXTR) NP_001341585.1:n.922+327_922+330delinsTGGA