Canonical Allele Identifier: CA369941440
Gene: VIPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034627C>A , CM000669.2:g.159034627C>A GRCh38
NC_000007.13:g.158827318C>A , CM000669.1:g.158827318C>A GRCh37
NC_000007.12:g.158520079C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.833G>T MANE Select ENSP00000262178.2:p.Ser278Ile
ENST00000262178.6:c.833G>T ENSP00000262178.2:p.Ser278Ile
ENST00000377633.7:c.785G>T ENSP00000366860.3:p.Ser262Ile
ENST00000402066.5:c.1256G>T ENSP00000384497.1:p.Ser419Ile
NM_001304522.1:c.593G>T NP_001291451.1:p.Ser198Ile
NM_001308259.1:c.785G>T NP_001295188.1:p.Ser262Ile
NM_003382.4:c.833G>T NP_003373.2:p.Ser278Ile
NR_130758.1:n.1019G>T
XM_005249561.2:c.908G>T XP_005249618.1:p.Ser303Ile
XM_006716107.1:c.833G>T XP_006716170.1:p.Ser278Ile
XM_006716108.2:c.644G>T XP_006716171.1:p.Ser215Ile
XM_011516550.1:c.785G>T XP_011514852.1:p.Ser262Ile
XM_011516552.1:c.419G>T XP_011514854.1:p.Ser140Ile
XR_242047.2:n.1228G>T
XM_005249561.3:c.908G>T XP_005249618.1:p.Ser303Ile
XM_006716107.2:c.833G>T XP_006716170.1:p.Ser278Ile
XM_006716108.3:c.644G>T XP_006716171.1:p.Ser215Ile
XM_011516550.2:c.785G>T XP_011514852.1:p.Ser262Ile
XM_017012580.1:c.419G>T XP_016868069.1:p.Ser140Ile
XM_024446914.1:c.908G>T XP_024302682.1:p.Ser303Ile
XM_024446915.1:c.908G>T XP_024302683.1:p.Ser303Ile
XM_024446916.1:c.833G>T XP_024302684.1:p.Ser278Ile
XM_024446917.1:c.644G>T XP_024302685.1:p.Ser215Ile
XM_024446918.1:c.419G>T XP_024302686.1:p.Ser140Ile
NM_003382.5:c.833G>T MANE Select NP_003373.2:p.Ser278Ile
NM_001304522.2:c.593G>T NP_001291451.1:p.Ser198Ile
NR_130758.2:n.929G>T