Canonical Allele Identifier: CA369941227

Gene: VIPR2

Linked Data

• dbSNP Id: rs1853805796
• MyVariant Identifiers: chr7:g.158827292G>T (hg19) ; chr7:g.159034601G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034601G>T , CM000669.2:g.159034601G>T	GRCh38
NC_000007.13:g.158827292G>T , CM000669.1:g.158827292G>T	GRCh37
NC_000007.12:g.158520053G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.859C>A MANE Select	ENSP00000262178.2:p.Pro287Thr
ENST00000262178.6:c.859C>A	ENSP00000262178.2:p.Pro287Thr
ENST00000377633.7:c.811C>A	ENSP00000366860.3:p.Pro271Thr
ENST00000402066.5:c.1282C>A	ENSP00000384497.1:p.Pro428Thr
NM_001304522.1:c.619C>A	NP_001291451.1:p.Pro207Thr
NM_001308259.1:c.811C>A	NP_001295188.1:p.Pro271Thr
NM_003382.4:c.859C>A	NP_003373.2:p.Pro287Thr
NR_130758.1:n.1045C>A
XM_005249561.2:c.934C>A	XP_005249618.1:p.Pro312Thr
XM_006716107.1:c.859C>A	XP_006716170.1:p.Pro287Thr
XM_006716108.2:c.670C>A	XP_006716171.1:p.Pro224Thr
XM_011516550.1:c.811C>A	XP_011514852.1:p.Pro271Thr
XM_011516552.1:c.445C>A	XP_011514854.1:p.Pro149Thr
XR_242047.2:n.1254C>A
XM_005249561.3:c.934C>A	XP_005249618.1:p.Pro312Thr
XM_006716107.2:c.859C>A	XP_006716170.1:p.Pro287Thr
XM_006716108.3:c.670C>A	XP_006716171.1:p.Pro224Thr
XM_011516550.2:c.811C>A	XP_011514852.1:p.Pro271Thr
XM_017012580.1:c.445C>A	XP_016868069.1:p.Pro149Thr
XM_024446914.1:c.934C>A	XP_024302682.1:p.Pro312Thr
XM_024446915.1:c.934C>A	XP_024302683.1:p.Pro312Thr
XM_024446916.1:c.859C>A	XP_024302684.1:p.Pro287Thr
XM_024446917.1:c.670C>A	XP_024302685.1:p.Pro224Thr
XM_024446918.1:c.445C>A	XP_024302686.1:p.Pro149Thr
NM_003382.5:c.859C>A MANE Select	NP_003373.2:p.Pro287Thr
NM_001304522.2:c.619C>A	NP_001291451.1:p.Pro207Thr
NR_130758.2:n.955C>A