Canonical Allele Identifier: CA1756436436

Gene: VIPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034347C= , CM000669.2:g.159034347C=	GRCh38
NC_000007.13:g.158827038C= , CM000669.1:g.158827038C=	GRCh37
NC_000007.12:g.158519799C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.880-43G= MANE Select	ENSP00000262178.2:n.880-43G=
ENST00000262178.6:c.880-43G=	ENSP00000262178.2:n.880-43G=
ENST00000377633.7:c.832-43G=	ENSP00000366860.3:n.832-43G=
ENST00000402066.5:c.1303-43G=	ENSP00000384497.1:n.1303-43G=
NM_001304522.1:c.640-43G=	NP_001291451.1:n.640-43G=
NM_001308259.1:c.832-43G=	NP_001295188.1:n.832-43G=
NM_003382.4:c.880-43G=	NP_003373.2:n.880-43G=
NR_130758.1:n.1066-43G=
XM_005249561.2:c.955-43G=	XP_005249618.1:n.955-43G=
XM_006716107.1:c.880-43G=	XP_006716170.1:n.880-43G=
XM_006716108.2:c.691-43G=	XP_006716171.1:n.691-43G=
XM_011516550.1:c.832-43G=	XP_011514852.1:n.832-43G=
XM_011516552.1:c.466-43G=	XP_011514854.1:n.466-43G=
XM_005249561.3:c.955-43G=	XP_005249618.1:n.955-43G=
XM_006716107.2:c.880-43G=	XP_006716170.1:n.880-43G=
XM_006716108.3:c.691-43G=	XP_006716171.1:n.691-43G=
XM_011516550.2:c.832-43G=	XP_011514852.1:n.832-43G=
XM_017012580.1:c.466-43G=	XP_016868069.1:n.466-43G=
XM_024446914.1:c.955-43G=	XP_024302682.1:n.955-43G=
XM_024446915.1:c.955-43G=	XP_024302683.1:n.955-43G=
XM_024446916.1:c.880-43G=	XP_024302684.1:n.880-43G=
XM_024446917.1:c.691-43G=	XP_024302685.1:n.691-43G=
XM_024446918.1:c.466-43G=	XP_024302686.1:n.466-43G=
NM_003382.5:c.880-43G= MANE Select	NP_003373.2:n.880-43G=
NM_001304522.2:c.640-43G=	NP_001291451.1:n.640-43G=
NR_130758.2:n.976-43G=