Canonical Allele Identifier: CA2664272697

Linked Data

gnomAD v4: 3-8767479-C-CA

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8767480dup , CM000665.2:g.8767480dup GRCh38
NC_000003.11:g.8809166dup , CM000665.1:g.8809166dup GRCh37
NC_000003.10:g.8784166dup NCBI36
NG_008797.2:g.38671dup , LRG_329:g.38671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.708dup (OXTR) MANE Select ENSP00000324270.2:p.Ala237CysfsTer?
ENST00000316793.7:c.708dup (OXTR) ENSP00000324270.2:p.Ala237CysfsTer?
ENST00000472766.1:n.156-9997dup (CAV3)
NM_000916.3:c.708dup (OXTR) NP_000907.2:p.Ala237CysfsTer?
XM_011533762.1:c.708dup (OXTR) XP_011532064.1:p.Ala237CysfsTer?
XM_011533763.1:c.708dup (OXTR) XP_011532065.1:p.Ala237CysfsTer?
NM_001354653.1:c.708dup (OXTR) NP_001341582.1:p.Ala237CysfsTer?
NM_001354654.1:c.708dup (OXTR) NP_001341583.1:p.Ala237CysfsTer?
NM_001354655.1:c.708dup (OXTR) NP_001341584.1:p.Ala237CysfsTer?
NM_001354656.1:c.708dup (OXTR) NP_001341585.1:p.Ala237CysfsTer?
NM_001354656.2:c.708dup (OXTR) NP_001341585.1:p.Ala237CysfsTer?
NM_000916.4:c.708dup (OXTR) MANE Select NP_000907.2:p.Ala237CysfsTer?
NM_001354653.2:c.708dup (OXTR) NP_001341582.1:p.Ala237CysfsTer?
NM_001354654.2:c.708dup (OXTR) NP_001341583.1:p.Ala237CysfsTer?
NM_001354655.2:c.708dup (OXTR) NP_001341584.1:p.Ala237CysfsTer?
NM_001354656.3:c.708dup (OXTR) NP_001341585.1:p.Ala237CysfsTer?