Canonical Allele Identifier: CA2755156455

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8767428_8767436del , CM000665.2:g.8767428_8767436del GRCh38
NC_000003.11:g.8809114_8809122del , CM000665.1:g.8809114_8809122del GRCh37
NC_000003.10:g.8784114_8784122del NCBI36
NG_008797.2:g.38619_38627del , LRG_329:g.38619_38627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316793.8:c.752_760del (OXTR) MANE Select ENSP00000324270.2:p.Asp251_Arg254delinsGly
ENST00000316793.7:c.752_760del (OXTR) ENSP00000324270.2:p.Asp251_Arg254delinsGly
ENST00000472766.1:n.156-10049_156-10041del (CAV3)
NM_000916.3:c.752_760del (OXTR) NP_000907.2:p.Asp251_Arg254delinsGly
XM_011533762.1:c.752_760del (OXTR) XP_011532064.1:p.Asp251_Arg254delinsGly
XM_011533763.1:c.752_760del (OXTR) XP_011532065.1:p.Asp251_Arg254delinsGly
NM_001354653.1:c.752_760del (OXTR) NP_001341582.1:p.Asp251_Arg254delinsGly
NM_001354654.1:c.752_760del (OXTR) NP_001341583.1:p.Asp251_Arg254delinsGly
NM_001354655.1:c.752_760del (OXTR) NP_001341584.1:p.Asp251_Arg254delinsGly
NM_001354656.1:c.752_760del (OXTR) NP_001341585.1:p.Asp251_Arg254delinsGly
NM_001354656.2:c.752_760del (OXTR) NP_001341585.1:p.Asp251_Arg254delinsGly
NM_000916.4:c.752_760del (OXTR) MANE Select NP_000907.2:p.Asp251_Arg254delinsGly
NM_001354653.2:c.752_760del (OXTR) NP_001341582.1:p.Asp251_Arg254delinsGly
NM_001354654.2:c.752_760del (OXTR) NP_001341583.1:p.Asp251_Arg254delinsGly
NM_001354655.2:c.752_760del (OXTR) NP_001341584.1:p.Asp251_Arg254delinsGly
NM_001354656.3:c.752_760del (OXTR) NP_001341585.1:p.Asp251_Arg254delinsGly