Canonical Allele Identifier: CA2664272694

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8767410_8767441del , CM000665.2:g.8767410_8767441del GRCh38
NC_000003.11:g.8809096_8809127del , CM000665.1:g.8809096_8809127del GRCh37
NC_000003.10:g.8784096_8784127del NCBI36
NG_008797.2:g.38601_38632del , LRG_329:g.38601_38632del

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.748_779del (OXTR) MANE Select ENSP00000324270.2:p.Gly250GlnfsTer?
ENST00000316793.7:c.748_779del (OXTR) ENSP00000324270.2:p.Gly250GlnfsTer?
ENST00000472766.1:n.156-10067_156-10036del (CAV3)
NM_000916.3:c.748_779del (OXTR) NP_000907.2:p.Gly250GlnfsTer?
XM_011533762.1:c.748_779del (OXTR) XP_011532064.1:p.Gly250GlnfsTer?
XM_011533763.1:c.748_779del (OXTR) XP_011532065.1:p.Gly250GlnfsTer?
NM_001354653.1:c.748_779del (OXTR) NP_001341582.1:p.Gly250GlnfsTer?
NM_001354654.1:c.748_779del (OXTR) NP_001341583.1:p.Gly250GlnfsTer?
NM_001354655.1:c.748_779del (OXTR) NP_001341584.1:p.Gly250GlnfsTer?
NM_001354656.1:c.748_779del (OXTR) NP_001341585.1:p.Gly250GlnfsTer?
NM_001354656.2:c.748_779del (OXTR) NP_001341585.1:p.Gly250GlnfsTer?
NM_000916.4:c.748_779del (OXTR) MANE Select NP_000907.2:p.Gly250GlnfsTer?
NM_001354653.2:c.748_779del (OXTR) NP_001341582.1:p.Gly250GlnfsTer?
NM_001354654.2:c.748_779del (OXTR) NP_001341583.1:p.Gly250GlnfsTer?
NM_001354655.2:c.748_779del (OXTR) NP_001341584.1:p.Gly250GlnfsTer?
NM_001354656.3:c.748_779del (OXTR) NP_001341585.1:p.Gly250GlnfsTer?