Canonical Allele Identifier: CA351664710

Gene: OXTR CAV3

Linked Data

• gnomAD v4: 3-8767407-T-C
• MyVariant Identifiers: chr3:g.8809093T>C (hg19) ; chr3:g.8767407T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8767407T>C , CM000665.2:g.8767407T>C	GRCh38
NC_000003.11:g.8809093T>C , CM000665.1:g.8809093T>C	GRCh37
NC_000003.10:g.8784093T>C	NCBI36
NG_008797.2:g.38598T>C , LRG_329:g.38598T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316793.8:c.781A>G (OXTR) MANE Select	ENSP00000324270.2:p.Ser261Gly
ENST00000316793.7:c.781A>G (OXTR)	ENSP00000324270.2:p.Ser261Gly
ENST00000472766.1:n.156-10070T>C (CAV3)
NM_000916.3:c.781A>G (OXTR)	NP_000907.2:p.Ser261Gly
XM_011533762.1:c.781A>G (OXTR)	XP_011532064.1:p.Ser261Gly
XM_011533763.1:c.781A>G (OXTR)	XP_011532065.1:p.Ser261Gly
NM_001354653.1:c.781A>G (OXTR)	NP_001341582.1:p.Ser261Gly
NM_001354654.1:c.781A>G (OXTR)	NP_001341583.1:p.Ser261Gly
NM_001354655.1:c.781A>G (OXTR)	NP_001341584.1:p.Ser261Gly
NM_001354656.1:c.781A>G (OXTR)	NP_001341585.1:p.Ser261Gly
NM_001354656.2:c.781A>G (OXTR)	NP_001341585.1:p.Ser261Gly
NM_000916.4:c.781A>G (OXTR) MANE Select	NP_000907.2:p.Ser261Gly
NM_001354653.2:c.781A>G (OXTR)	NP_001341582.1:p.Ser261Gly
NM_001354654.2:c.781A>G (OXTR)	NP_001341583.1:p.Ser261Gly
NM_001354655.2:c.781A>G (OXTR)	NP_001341584.1:p.Ser261Gly
NM_001354656.3:c.781A>G (OXTR)	NP_001341585.1:p.Ser261Gly