Canonical Allele Identifier: CA1344416657

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768730_8768731delinsAC , CM000665.2:g.8768730_8768731delinsAC GRCh38
NC_000003.11:g.8810416_8810417delinsAC , CM000665.1:g.8810416_8810417delinsAC GRCh37
NC_000003.10:g.8785416_8785417delinsAC NCBI36
NG_008797.2:g.39921_39922delinsAC , LRG_329:g.39921_39922delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.-238-140_-238-139delinsGT (OXTR) MANE Select ENSP00000324270.2:n.-238-140_-238-139deli...
ENST00000316793.7:c.-238-140_-238-139delinsGT (OXTR) ENSP00000324270.2:n.-238-140_-238-139deli...
ENST00000431493.1:c.-238-140_-238-139delinsGT (OXTR) ENSP00000414828.1:n.-238-140_-238-139deli...
ENST00000472766.1:n.156-8747_156-8746delinsAC (CAV3)
ENST00000474615.1:n.384-140_384-139delinsGT (OXTR)
NM_000916.3:c.-238-140_-238-139delinsGT (OXTR) NP_000907.2:n.-238-140_-238-139delinsGT
XM_011533762.1:c.-238-140_-238-139delinsGT (OXTR) XP_011532064.1:n.-238-140_-238-139delinsG...
XM_011533763.1:c.-238-140_-238-139delinsGT (OXTR) XP_011532065.1:n.-238-140_-238-139delinsG...
NM_001354653.1:c.-238-140_-238-139delinsGT (OXTR) NP_001341582.1:n.-238-140_-238-139delinsG...
NM_001354654.1:c.-238-140_-238-139delinsGT (OXTR) NP_001341583.1:n.-238-140_-238-139delinsG...
NM_001354655.1:c.-238-140_-238-139delinsGT (OXTR) NP_001341584.1:n.-238-140_-238-139delinsG...
NM_001354656.2:c.-282_-281delinsGT (OXTR) NP_001341585.1:n.-282_-281delinsGT
NM_000916.4:c.-238-140_-238-139delinsGT (OXTR) MANE Select NP_000907.2:n.-238-140_-238-139delinsGT
NM_001354653.2:c.-238-140_-238-139delinsGT (OXTR) NP_001341582.1:n.-238-140_-238-139delinsG...
NM_001354654.2:c.-238-140_-238-139delinsGT (OXTR) NP_001341583.1:n.-238-140_-238-139delinsG...
NM_001354655.2:c.-238-140_-238-139delinsGT (OXTR) NP_001341584.1:n.-238-140_-238-139delinsG...
NM_001354656.3:c.-282_-281delinsGT (OXTR) NP_001341585.1:n.-282_-281delinsGT