Canonical Allele Identifier: CA1756436778

Gene: VIPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034599C= , CM000669.2:g.159034599C=	GRCh38
NC_000007.13:g.158827290C= , CM000669.1:g.158827290C=	GRCh37
NC_000007.12:g.158520051C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.861G= MANE Select	ENSP00000262178.2:p.Pro287=
ENST00000262178.6:c.861G=	ENSP00000262178.2:p.Pro287=
ENST00000377633.7:c.813G=	ENSP00000366860.3:p.Pro271=
ENST00000402066.5:c.1284G=	ENSP00000384497.1:p.Pro428=
NM_001304522.1:c.621G=	NP_001291451.1:p.Pro207=
NM_001308259.1:c.813G=	NP_001295188.1:p.Pro271=
NM_003382.4:c.861G=	NP_003373.2:p.Pro287=
NR_130758.1:n.1047G=
XM_005249561.2:c.936G=	XP_005249618.1:p.Pro312=
XM_006716107.1:c.861G=	XP_006716170.1:p.Pro287=
XM_006716108.2:c.672G=	XP_006716171.1:p.Pro224=
XM_011516550.1:c.813G=	XP_011514852.1:p.Pro271=
XM_011516552.1:c.447G=	XP_011514854.1:p.Pro149=
XR_242047.2:n.1256G=
XM_005249561.3:c.936G=	XP_005249618.1:p.Pro312=
XM_006716107.2:c.861G=	XP_006716170.1:p.Pro287=
XM_006716108.3:c.672G=	XP_006716171.1:p.Pro224=
XM_011516550.2:c.813G=	XP_011514852.1:p.Pro271=
XM_017012580.1:c.447G=	XP_016868069.1:p.Pro149=
XM_024446914.1:c.936G=	XP_024302682.1:p.Pro312=
XM_024446915.1:c.936G=	XP_024302683.1:p.Pro312=
XM_024446916.1:c.861G=	XP_024302684.1:p.Pro287=
XM_024446917.1:c.672G=	XP_024302685.1:p.Pro224=
XM_024446918.1:c.447G=	XP_024302686.1:p.Pro149=
NM_003382.5:c.861G= MANE Select	NP_003373.2:p.Pro287=
NM_001304522.2:c.621G=	NP_001291451.1:p.Pro207=
NR_130758.2:n.957G=