Canonical Allele Identifier: CA1344416765

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768931_8768932delinsAC , CM000665.2:g.8768931_8768932delinsAC GRCh38
NC_000003.11:g.8810617_8810618delinsAC , CM000665.1:g.8810617_8810618delinsAC GRCh37
NC_000003.10:g.8785617_8785618delinsAC NCBI36
NG_008797.2:g.40122_40123delinsAC , LRG_329:g.40122_40123delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.-239+299_-239+300delinsGT (OXTR) MANE Select ENSP00000324270.2:n.-239+299_-239+300delinsGT
ENST00000316793.7:c.-239+299_-239+300delinsGT (OXTR) ENSP00000324270.2:n.-239+299_-239+300delinsGT
ENST00000431493.1:c.-239+322_-239+323delinsGT (OXTR) ENSP00000414828.1:n.-239+322_-239+323delinsGT
ENST00000472766.1:n.156-8546_156-8545delinsAC (CAV3)
ENST00000474615.1:n.383+299_383+300delinsGT (OXTR)
NM_000916.3:c.-239+299_-239+300delinsGT (OXTR) NP_000907.2:n.-239+299_-239+300delinsGT
XM_011533762.1:c.-239+322_-239+323delinsGT (OXTR) XP_011532064.1:n.-239+322_-239+323delinsGT
XM_011533763.1:c.-238-341_-238-340delinsGT (OXTR) XP_011532065.1:n.-238-341_-238-340delinsGT
NM_001354653.1:c.-239+299_-239+300delinsGT (OXTR) NP_001341582.1:n.-239+299_-239+300delinsGT
NM_001354654.1:c.-239+322_-239+323delinsGT (OXTR) NP_001341583.1:n.-239+322_-239+323delinsGT
NM_001354655.1:c.-239+116_-239+117delinsGT (OXTR) NP_001341584.1:n.-239+116_-239+117delinsGT
NM_000916.4:c.-239+299_-239+300delinsGT (OXTR) MANE Select NP_000907.2:n.-239+299_-239+300delinsGT
NM_001354653.2:c.-239+299_-239+300delinsGT (OXTR) NP_001341582.1:n.-239+299_-239+300delinsGT
NM_001354654.2:c.-239+322_-239+323delinsGT (OXTR) NP_001341583.1:n.-239+322_-239+323delinsGT
NM_001354655.2:c.-239+116_-239+117delinsGT (OXTR) NP_001341584.1:n.-239+116_-239+117delinsGT