Canonical Allele Identifier: CA1344416802

Gene: OXTR CAV3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8769003C= , CM000665.2:g.8769003C=	GRCh38
NC_000003.11:g.8810689C= , CM000665.1:g.8810689C=	GRCh37
NC_000003.10:g.8785689C=	NCBI36
NG_008797.2:g.40194C= , LRG_329:g.40194C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316793.8:c.-239+228G= (OXTR) MANE Select	ENSP00000324270.2:n.-239+228G=
ENST00000316793.7:c.-239+228G= (OXTR)	ENSP00000324270.2:n.-239+228G=
ENST00000431493.1:c.-239+251G= (OXTR)	ENSP00000414828.1:n.-239+251G=
ENST00000472766.1:n.156-8474C= (CAV3)
ENST00000474615.1:n.383+228G= (OXTR)
NM_000916.3:c.-239+228G= (OXTR)	NP_000907.2:n.-239+228G=
XM_011533762.1:c.-239+251G= (OXTR)	XP_011532064.1:n.-239+251G=
XM_011533763.1:c.-238-412G= (OXTR)	XP_011532065.1:n.-238-412G=
NM_001354653.1:c.-239+228G= (OXTR)	NP_001341582.1:n.-239+228G=
NM_001354654.1:c.-239+251G= (OXTR)	NP_001341583.1:n.-239+251G=
NM_001354655.1:c.-239+45G= (OXTR)	NP_001341584.1:n.-239+45G=
NM_000916.4:c.-239+228G= (OXTR) MANE Select	NP_000907.2:n.-239+228G=
NM_001354653.2:c.-239+228G= (OXTR)	NP_001341582.1:n.-239+228G=
NM_001354654.2:c.-239+251G= (OXTR)	NP_001341583.1:n.-239+251G=
NM_001354655.2:c.-239+45G= (OXTR)	NP_001341584.1:n.-239+45G=