Canonical Allele Identifier: CA2664273316

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8768648_8768654del , CM000665.2:g.8768648_8768654del GRCh38
NC_000003.11:g.8810334_8810340del , CM000665.1:g.8810334_8810340del GRCh37
NC_000003.10:g.8785334_8785340del NCBI36
NG_008797.2:g.39839_39845del , LRG_329:g.39839_39845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.-238-61_-238-55del (OXTR) MANE Select ENSP00000324270.2:n.-238-61_-238-55del
ENST00000316793.7:c.-238-61_-238-55del (OXTR) ENSP00000324270.2:n.-238-61_-238-55del
ENST00000431493.1:c.-238-61_-238-55del (OXTR) ENSP00000414828.1:n.-238-61_-238-55del
ENST00000449615.1:c.-299_-293del (OXTR) ENSP00000389587.1:n.-299_-293del
ENST00000472766.1:n.156-8829_156-8823del (CAV3)
ENST00000474615.1:n.384-61_384-55del (OXTR)
NM_000916.3:c.-238-61_-238-55del (OXTR) NP_000907.2:n.-238-61_-238-55del
XM_011533762.1:c.-238-61_-238-55del (OXTR) XP_011532064.1:n.-238-61_-238-55del
XM_011533763.1:c.-238-61_-238-55del (OXTR) XP_011532065.1:n.-238-61_-238-55del
NM_001354653.1:c.-238-61_-238-55del (OXTR) NP_001341582.1:n.-238-61_-238-55del
NM_001354654.1:c.-238-61_-238-55del (OXTR) NP_001341583.1:n.-238-61_-238-55del
NM_001354655.1:c.-238-61_-238-55del (OXTR) NP_001341584.1:n.-238-61_-238-55del
NM_001354656.1:c.-239+36_-239+42del (OXTR) NP_001341585.1:n.-239+36_-239+42del
NM_001354656.2:c.-239+36_-239+42del (OXTR) NP_001341585.1:n.-239+36_-239+42del
NM_000916.4:c.-238-61_-238-55del (OXTR) MANE Select NP_000907.2:n.-238-61_-238-55del
NM_001354653.2:c.-238-61_-238-55del (OXTR) NP_001341582.1:n.-238-61_-238-55del
NM_001354654.2:c.-238-61_-238-55del (OXTR) NP_001341583.1:n.-238-61_-238-55del
NM_001354655.2:c.-238-61_-238-55del (OXTR) NP_001341584.1:n.-238-61_-238-55del
NM_001354656.3:c.-239+36_-239+42del (OXTR) NP_001341585.1:n.-239+36_-239+42del