Canonical Allele Identifier: CA2664272710

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768139_8768240del , CM000665.2:g.8768139_8768240del GRCh38
NC_000003.11:g.8809825_8809926del , CM000665.1:g.8809825_8809926del GRCh37
NC_000003.10:g.8784825_8784926del NCBI36
NG_008797.2:g.39330_39431del , LRG_329:g.39330_39431del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.-48_54del (OXTR)
ENST00000316793.7:c.-48_54del (OXTR)
ENST00000431493.1:c.-48_54del (OXTR)
ENST00000449615.1:c.-48_54del (OXTR)
ENST00000472766.1:n.156-9338_156-9237del (CAV3)
NM_000916.3:c.-48_54del (OXTR)
XM_011533762.1:c.-48_54del (OXTR)
XM_011533763.1:c.-48_54del (OXTR)
NM_001354653.1:c.-48_54del (OXTR)
NM_001354654.1:c.-48_54del (OXTR)
NM_001354655.1:c.-48_54del (OXTR)
NM_001354656.1:c.-48_54del (OXTR)
NM_001354656.2:c.-48_54del (OXTR)
NM_000916.4:c.-48_54del (OXTR)
NM_001354653.2:c.-48_54del (OXTR)
NM_001354654.2:c.-48_54del (OXTR)
NM_001354655.2:c.-48_54del (OXTR)
NM_001354656.3:c.-48_54del (OXTR)