Canonical Allele Identifier: CA1756436870

Gene: VIPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034631G= , CM000669.2:g.159034631G=	GRCh38
NC_000007.13:g.158827322G= , CM000669.1:g.158827322G=	GRCh37
NC_000007.12:g.158520083G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.829C= MANE Select	ENSP00000262178.2:p.His277=
ENST00000262178.6:c.829C=	ENSP00000262178.2:p.His277=
ENST00000377633.7:c.781C=	ENSP00000366860.3:p.His261=
ENST00000402066.5:c.1252C=	ENSP00000384497.1:p.His418=
NM_001304522.1:c.589C=	NP_001291451.1:p.His197=
NM_001308259.1:c.781C=	NP_001295188.1:p.His261=
NM_003382.4:c.829C=	NP_003373.2:p.His277=
NR_130758.1:n.1015C=
XM_005249561.2:c.904C=	XP_005249618.1:p.His302=
XM_006716107.1:c.829C=	XP_006716170.1:p.His277=
XM_006716108.2:c.640C=	XP_006716171.1:p.His214=
XM_011516550.1:c.781C=	XP_011514852.1:p.His261=
XM_011516552.1:c.415C=	XP_011514854.1:p.His139=
XR_242047.2:n.1224C=
XM_005249561.3:c.904C=	XP_005249618.1:p.His302=
XM_006716107.2:c.829C=	XP_006716170.1:p.His277=
XM_006716108.3:c.640C=	XP_006716171.1:p.His214=
XM_011516550.2:c.781C=	XP_011514852.1:p.His261=
XM_017012580.1:c.415C=	XP_016868069.1:p.His139=
XM_024446914.1:c.904C=	XP_024302682.1:p.His302=
XM_024446915.1:c.904C=	XP_024302683.1:p.His302=
XM_024446916.1:c.829C=	XP_024302684.1:p.His277=
XM_024446917.1:c.640C=	XP_024302685.1:p.His214=
XM_024446918.1:c.415C=	XP_024302686.1:p.His139=
NM_003382.5:c.829C= MANE Select	NP_003373.2:p.His277=
NM_001304522.2:c.589C=	NP_001291451.1:p.His197=
NR_130758.2:n.925C=