Canonical Allele Identifier: CA1344412489

Gene: OXTR CAV3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8760904_8760905delinsTA , CM000665.2:g.8760904_8760905delinsTA	GRCh38
NC_000003.11:g.8802590_8802591delinsTA , CM000665.1:g.8802590_8802591delinsTA	GRCh37
NC_000003.10:g.8777590_8777591delinsTA	NCBI36
NG_008797.2:g.32095_32096delinsTA , LRG_329:g.32095_32096delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000316793.8:c.922+6361_922+6362delinsTA (OXTR) MANE Select	ENSP00000324270.2:n.922+6361_922+6362deli...
ENST00000316793.7:c.922+6361_922+6362delinsTA (OXTR)	ENSP00000324270.2:n.922+6361_922+6362deli...
ENST00000472766.1:n.156-16573_156-16572delinsTA (CAV3)
NM_000916.3:c.922+6361_922+6362delinsTA (OXTR)	NP_000907.2:n.922+6361_922+6362delinsTA
XM_011533762.1:c.922+6361_922+6362delinsTA (OXTR)	XP_011532064.1:n.922+6361_922+6362delinsT...
XM_011533763.1:c.922+6361_922+6362delinsTA (OXTR)	XP_011532065.1:n.922+6361_922+6362delinsT...
NM_001354653.1:c.922+6361_922+6362delinsTA (OXTR)	NP_001341582.1:n.922+6361_922+6362delinsT...
NM_001354654.1:c.922+6361_922+6362delinsTA (OXTR)	NP_001341583.1:n.922+6361_922+6362delinsT...
NM_001354655.1:c.922+6361_922+6362delinsTA (OXTR)	NP_001341584.1:n.922+6361_922+6362delinsT...
NM_001354656.1:c.922+6361_922+6362delinsTA (OXTR)	NP_001341585.1:n.922+6361_922+6362delinsT...
NM_001354656.2:c.922+6361_922+6362delinsTA (OXTR)	NP_001341585.1:n.922+6361_922+6362delinsT...
NM_000916.4:c.922+6361_922+6362delinsTA (OXTR) MANE Select	NP_000907.2:n.922+6361_922+6362delinsTA
NM_001354653.2:c.922+6361_922+6362delinsTA (OXTR)	NP_001341582.1:n.922+6361_922+6362delinsT...
NM_001354654.2:c.922+6361_922+6362delinsTA (OXTR)	NP_001341583.1:n.922+6361_922+6362delinsT...
NM_001354655.2:c.922+6361_922+6362delinsTA (OXTR)	NP_001341584.1:n.922+6361_922+6362delinsT...
NM_001354656.3:c.922+6361_922+6362delinsTA (OXTR)	NP_001341585.1:n.922+6361_922+6362delinsT...