Canonical Allele Identifier: CA1344413772

Gene: OXTR CAV3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8762832_8762836delinsCCTTT , CM000665.2:g.8762832_8762836delinsCCTTT	GRCh38
NC_000003.11:g.8804518_8804522delinsCCTTT , CM000665.1:g.8804518_8804522delinsCCTTT	GRCh37
NC_000003.10:g.8779518_8779522delinsCCTTT	NCBI36
NG_008797.2:g.34023_34027delinsCCTTT , LRG_329:g.34023_34027delinsCCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000316793.8:c.922+4430_922+4434delinsAAAGG (OXTR) MANE Select	ENSP00000324270.2:n.922+4430_922+4434deli...
ENST00000316793.7:c.922+4430_922+4434delinsAAAGG (OXTR)	ENSP00000324270.2:n.922+4430_922+4434deli...
ENST00000472766.1:n.156-14645_156-14641delinsCCTTT (CAV3)
NM_000916.3:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_000907.2:n.922+4430_922+4434delinsAAAG...
XM_011533762.1:c.922+4430_922+4434delinsAAAGG (OXTR)	XP_011532064.1:n.922+4430_922+4434delinsA...
XM_011533763.1:c.922+4430_922+4434delinsAAAGG (OXTR)	XP_011532065.1:n.922+4430_922+4434delinsA...
NM_001354653.1:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341582.1:n.922+4430_922+4434delinsA...
NM_001354654.1:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341583.1:n.922+4430_922+4434delinsA...
NM_001354655.1:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341584.1:n.922+4430_922+4434delinsA...
NM_001354656.1:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341585.1:n.922+4430_922+4434delinsA...
NM_001354656.2:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341585.1:n.922+4430_922+4434delinsA...
NM_000916.4:c.922+4430_922+4434delinsAAAGG (OXTR) MANE Select	NP_000907.2:n.922+4430_922+4434delinsAAAG...
NM_001354653.2:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341582.1:n.922+4430_922+4434delinsA...
NM_001354654.2:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341583.1:n.922+4430_922+4434delinsA...
NM_001354655.2:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341584.1:n.922+4430_922+4434delinsA...
NM_001354656.3:c.922+4430_922+4434delinsAAAGG (OXTR)	NP_001341585.1:n.922+4430_922+4434delinsA...