Canonical Allele Identifier: CA1344408282

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8755398_8755399delinsGC , CM000665.2:g.8755398_8755399delinsGC GRCh38
NC_000003.11:g.8797084_8797085delinsGC , CM000665.1:g.8797084_8797085delinsGC GRCh37
NC_000003.10:g.8772084_8772085delinsGC NCBI36
NG_008797.2:g.26589_26590delinsGC , LRG_329:g.26589_26590delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000316793.8:c.923-2175_923-2174delinsGC (OXTR) MANE Select ENSP00000324270.2:n.923-2175_923-2174deli...
ENST00000316793.7:c.923-2175_923-2174delinsGC (OXTR) ENSP00000324270.2:n.923-2175_923-2174deli...
ENST00000472766.1:n.155+21408_155+21409delinsGC (CAV3)
NM_000916.3:c.923-2175_923-2174delinsGC (OXTR) NP_000907.2:n.923-2175_923-2174delinsGC
XM_011533762.1:c.923-2175_923-2174delinsGC (OXTR) XP_011532064.1:n.923-2175_923-2174delinsG...
XM_011533763.1:c.923-2175_923-2174delinsGC (OXTR) XP_011532065.1:n.923-2175_923-2174delinsG...
NM_001354653.1:c.923-2175_923-2174delinsGC (OXTR) NP_001341582.1:n.923-2175_923-2174delinsG...
NM_001354654.1:c.923-2175_923-2174delinsGC (OXTR) NP_001341583.1:n.923-2175_923-2174delinsG...
NM_001354655.1:c.923-2175_923-2174delinsGC (OXTR) NP_001341584.1:n.923-2175_923-2174delinsG...
NM_001354656.1:c.923-2175_923-2174delinsGC (OXTR) NP_001341585.1:n.923-2175_923-2174delinsG...
NM_001354656.2:c.923-2175_923-2174delinsGC (OXTR) NP_001341585.1:n.923-2175_923-2174delinsG...
NM_000916.4:c.923-2175_923-2174delinsGC (OXTR) MANE Select NP_000907.2:n.923-2175_923-2174delinsGC
NM_001354653.2:c.923-2175_923-2174delinsGC (OXTR) NP_001341582.1:n.923-2175_923-2174delinsG...
NM_001354654.2:c.923-2175_923-2174delinsGC (OXTR) NP_001341583.1:n.923-2175_923-2174delinsG...
NM_001354655.2:c.923-2175_923-2174delinsGC (OXTR) NP_001341584.1:n.923-2175_923-2174delinsG...
NM_001354656.3:c.923-2175_923-2174delinsGC (OXTR) NP_001341585.1:n.923-2175_923-2174delinsG...