Canonical Allele Identifier: CA369941386
Gene: VIPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1469864554

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034621G>A , CM000669.2:g.159034621G>A GRCh38
NC_000007.13:g.158827312G>A , CM000669.1:g.158827312G>A GRCh37
NC_000007.12:g.158520073G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.839C>T MANE Select ENSP00000262178.2:p.Pro280Leu
ENST00000262178.6:c.839C>T ENSP00000262178.2:p.Pro280Leu
ENST00000377633.7:c.791C>T ENSP00000366860.3:p.Pro264Leu
ENST00000402066.5:c.1262C>T ENSP00000384497.1:p.Pro421Leu
NM_001304522.1:c.599C>T NP_001291451.1:p.Pro200Leu
NM_001308259.1:c.791C>T NP_001295188.1:p.Pro264Leu
NM_003382.4:c.839C>T NP_003373.2:p.Pro280Leu
NR_130758.1:n.1025C>T
XM_005249561.2:c.914C>T XP_005249618.1:p.Pro305Leu
XM_006716107.1:c.839C>T XP_006716170.1:p.Pro280Leu
XM_006716108.2:c.650C>T XP_006716171.1:p.Pro217Leu
XM_011516550.1:c.791C>T XP_011514852.1:p.Pro264Leu
XM_011516552.1:c.425C>T XP_011514854.1:p.Pro142Leu
XR_242047.2:n.1234C>T
XM_005249561.3:c.914C>T XP_005249618.1:p.Pro305Leu
XM_006716107.2:c.839C>T XP_006716170.1:p.Pro280Leu
XM_006716108.3:c.650C>T XP_006716171.1:p.Pro217Leu
XM_011516550.2:c.791C>T XP_011514852.1:p.Pro264Leu
XM_017012580.1:c.425C>T XP_016868069.1:p.Pro142Leu
XM_024446914.1:c.914C>T XP_024302682.1:p.Pro305Leu
XM_024446915.1:c.914C>T XP_024302683.1:p.Pro305Leu
XM_024446916.1:c.839C>T XP_024302684.1:p.Pro280Leu
XM_024446917.1:c.650C>T XP_024302685.1:p.Pro217Leu
XM_024446918.1:c.425C>T XP_024302686.1:p.Pro142Leu
NM_003382.5:c.839C>T MANE Select NP_003373.2:p.Pro280Leu
NM_001304522.2:c.599C>T NP_001291451.1:p.Pro200Leu
NR_130758.2:n.935C>T