Canonical Allele Identifier: CA1044892282

Linked Data

dbSNP Id: rs1708703642

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768964_8768965insAGCG , CM000665.2:g.8768964_8768965insAGCG GRCh38
NC_000003.11:g.8810650_8810651insAGCG , CM000665.1:g.8810650_8810651insAGCG GRCh37
NC_000003.10:g.8785650_8785651insAGCG NCBI36
NG_008797.2:g.40155_40156insAGCG , LRG_329:g.40155_40156insAGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.-239+266_-239+267insCGCT (OXTR) MANE Select ENSP00000324270.2:n.-239+266_-239+267insCGCT
ENST00000316793.7:c.-239+266_-239+267insCGCT (OXTR) ENSP00000324270.2:n.-239+266_-239+267insCGCT
ENST00000431493.1:c.-239+289_-239+290insCGCT (OXTR) ENSP00000414828.1:n.-239+289_-239+290insCGCT
ENST00000472766.1:n.156-8513_156-8512insAGCG (CAV3)
ENST00000474615.1:n.383+266_383+267insCGCT (OXTR)
NM_000916.3:c.-239+266_-239+267insCGCT (OXTR) NP_000907.2:n.-239+266_-239+267insCGCT
XM_011533762.1:c.-239+289_-239+290insCGCT (OXTR) XP_011532064.1:n.-239+289_-239+290insCGCT
XM_011533763.1:c.-238-374_-238-373insCGCT (OXTR) XP_011532065.1:n.-238-374_-238-373insCGCT
NM_001354653.1:c.-239+266_-239+267insCGCT (OXTR) NP_001341582.1:n.-239+266_-239+267insCGCT
NM_001354654.1:c.-239+289_-239+290insCGCT (OXTR) NP_001341583.1:n.-239+289_-239+290insCGCT
NM_001354655.1:c.-239+83_-239+84insCGCT (OXTR) NP_001341584.1:n.-239+83_-239+84insCGCT
NM_000916.4:c.-239+266_-239+267insCGCT (OXTR) MANE Select NP_000907.2:n.-239+266_-239+267insCGCT
NM_001354653.2:c.-239+266_-239+267insCGCT (OXTR) NP_001341582.1:n.-239+266_-239+267insCGCT
NM_001354654.2:c.-239+289_-239+290insCGCT (OXTR) NP_001341583.1:n.-239+289_-239+290insCGCT
NM_001354655.2:c.-239+83_-239+84insCGCT (OXTR) NP_001341584.1:n.-239+83_-239+84insCGCT