Canonical Allele Identifier: CA1756436577

Gene: VIPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034444_159034445delinsCT , CM000669.2:g.159034444_159034445delinsCT	GRCh38
NC_000007.13:g.158827135_158827136delinsCT , CM000669.1:g.158827135_158827136delinsCT	GRCh37
NC_000007.12:g.158519896_158519897delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.879+136_879+137delinsAG MANE Select	ENSP00000262178.2:n.879+136_879+137delinsAG
ENST00000262178.6:c.879+136_879+137delinsAG	ENSP00000262178.2:n.879+136_879+137delinsAG
ENST00000377633.7:c.831+136_831+137delinsAG	ENSP00000366860.3:n.831+136_831+137delinsAG
ENST00000402066.5:c.1302+136_1302+137delinsAG	ENSP00000384497.1:n.1302+136_1302+137delinsAG
NM_001304522.1:c.639+136_639+137delinsAG	NP_001291451.1:n.639+136_639+137delinsAG
NM_001308259.1:c.831+136_831+137delinsAG	NP_001295188.1:n.831+136_831+137delinsAG
NM_003382.4:c.879+136_879+137delinsAG	NP_003373.2:n.879+136_879+137delinsAG
NR_130758.1:n.1065+136_1065+137delinsAG
XM_005249561.2:c.954+136_954+137delinsAG	XP_005249618.1:n.954+136_954+137delinsAG
XM_006716107.1:c.879+136_879+137delinsAG	XP_006716170.1:n.879+136_879+137delinsAG
XM_006716108.2:c.690+136_690+137delinsAG	XP_006716171.1:n.690+136_690+137delinsAG
XM_011516550.1:c.831+136_831+137delinsAG	XP_011514852.1:n.831+136_831+137delinsAG
XM_011516552.1:c.465+136_465+137delinsAG	XP_011514854.1:n.465+136_465+137delinsAG
XM_005249561.3:c.954+136_954+137delinsAG	XP_005249618.1:n.954+136_954+137delinsAG
XM_006716107.2:c.879+136_879+137delinsAG	XP_006716170.1:n.879+136_879+137delinsAG
XM_006716108.3:c.690+136_690+137delinsAG	XP_006716171.1:n.690+136_690+137delinsAG
XM_011516550.2:c.831+136_831+137delinsAG	XP_011514852.1:n.831+136_831+137delinsAG
XM_017012580.1:c.465+136_465+137delinsAG	XP_016868069.1:n.465+136_465+137delinsAG
XM_024446914.1:c.954+136_954+137delinsAG	XP_024302682.1:n.954+136_954+137delinsAG
XM_024446915.1:c.954+136_954+137delinsAG	XP_024302683.1:n.954+136_954+137delinsAG
XM_024446916.1:c.879+136_879+137delinsAG	XP_024302684.1:n.879+136_879+137delinsAG
XM_024446917.1:c.690+136_690+137delinsAG	XP_024302685.1:n.690+136_690+137delinsAG
XM_024446918.1:c.465+136_465+137delinsAG	XP_024302686.1:n.465+136_465+137delinsAG
NM_003382.5:c.879+136_879+137delinsAG MANE Select	NP_003373.2:n.879+136_879+137delinsAG
NM_001304522.2:c.639+136_639+137delinsAG	NP_001291451.1:n.639+136_639+137delinsAG
NR_130758.2:n.975+136_975+137delinsAG