Canonical Allele Identifier: CA2685895350

Gene: VIPR2

Linked Data

• gnomAD v4: 7-159034466-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034467_159034468dup , CM000669.2:g.159034467_159034468dup	GRCh38
NC_000007.13:g.158827158_158827159dup , CM000669.1:g.158827158_158827159dup	GRCh37
NC_000007.12:g.158519919_158519920dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.879+113_879+114dup MANE Select	ENSP00000262178.2:n.879+113_879+114dup
ENST00000262178.6:c.879+113_879+114dup	ENSP00000262178.2:n.879+113_879+114dup
ENST00000377633.7:c.831+113_831+114dup	ENSP00000366860.3:n.831+113_831+114dup
ENST00000402066.5:c.1302+113_1302+114dup	ENSP00000384497.1:n.1302+113_1302+114dup
NM_001304522.1:c.639+113_639+114dup	NP_001291451.1:n.639+113_639+114dup
NM_001308259.1:c.831+113_831+114dup	NP_001295188.1:n.831+113_831+114dup
NM_003382.4:c.879+113_879+114dup	NP_003373.2:n.879+113_879+114dup
NR_130758.1:n.1065+113_1065+114dup
XM_005249561.2:c.954+113_954+114dup	XP_005249618.1:n.954+113_954+114dup
XM_006716107.1:c.879+113_879+114dup	XP_006716170.1:n.879+113_879+114dup
XM_006716108.2:c.690+113_690+114dup	XP_006716171.1:n.690+113_690+114dup
XM_011516550.1:c.831+113_831+114dup	XP_011514852.1:n.831+113_831+114dup
XM_011516552.1:c.465+113_465+114dup	XP_011514854.1:n.465+113_465+114dup
XM_005249561.3:c.954+113_954+114dup	XP_005249618.1:n.954+113_954+114dup
XM_006716107.2:c.879+113_879+114dup	XP_006716170.1:n.879+113_879+114dup
XM_006716108.3:c.690+113_690+114dup	XP_006716171.1:n.690+113_690+114dup
XM_011516550.2:c.831+113_831+114dup	XP_011514852.1:n.831+113_831+114dup
XM_017012580.1:c.465+113_465+114dup	XP_016868069.1:n.465+113_465+114dup
XM_024446914.1:c.954+113_954+114dup	XP_024302682.1:n.954+113_954+114dup
XM_024446915.1:c.954+113_954+114dup	XP_024302683.1:n.954+113_954+114dup
XM_024446916.1:c.879+113_879+114dup	XP_024302684.1:n.879+113_879+114dup
XM_024446917.1:c.690+113_690+114dup	XP_024302685.1:n.690+113_690+114dup
XM_024446918.1:c.465+113_465+114dup	XP_024302686.1:n.465+113_465+114dup
NM_003382.5:c.879+113_879+114dup MANE Select	NP_003373.2:n.879+113_879+114dup
NM_001304522.2:c.639+113_639+114dup	NP_001291451.1:n.639+113_639+114dup
NR_130758.2:n.975+113_975+114dup