Canonical Allele Identifier: CA1044892033

Gene: OXTR CAV3

Linked Data

• dbSNP Id: rs1708681461
• gnomAD v3: 3-8768165-TTGGCTGCGAGCGCGCCCTCCATGACCC-T
• gnomAD v4: 3-8768165-TTGGCTGCGAGCGCGCCCTCCATGACCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8768170_8768196del , CM000665.2:g.8768170_8768196del	GRCh38
NC_000003.11:g.8809856_8809882del , CM000665.1:g.8809856_8809882del	GRCh37
NC_000003.10:g.8784856_8784882del	NCBI36
NG_008797.2:g.39361_39387del , LRG_329:g.39361_39387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316793.8:c.-5_22del (OXTR)
ENST00000316793.7:c.-5_22del (OXTR)
ENST00000431493.1:c.-5_22del (OXTR)
ENST00000449615.1:c.-5_22del (OXTR)
ENST00000472766.1:n.156-9307_156-9281del (CAV3)
NM_000916.3:c.-5_22del (OXTR)
XM_011533762.1:c.-5_22del (OXTR)
XM_011533763.1:c.-5_22del (OXTR)
NM_001354653.1:c.-5_22del (OXTR)
NM_001354654.1:c.-5_22del (OXTR)
NM_001354655.1:c.-5_22del (OXTR)
NM_001354656.1:c.-5_22del (OXTR)
NM_001354656.2:c.-5_22del (OXTR)
NM_000916.4:c.-5_22del (OXTR)
NM_001354653.2:c.-5_22del (OXTR)
NM_001354654.2:c.-5_22del (OXTR)
NM_001354655.2:c.-5_22del (OXTR)
NM_001354656.3:c.-5_22del (OXTR)