Canonical Allele Identifier: CA369941411
Gene: VIPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034624A>T , CM000669.2:g.159034624A>T GRCh38
NC_000007.13:g.158827315A>T , CM000669.1:g.158827315A>T GRCh37
NC_000007.12:g.158520076A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.836T>A MANE Select ENSP00000262178.2:p.Val279Glu
ENST00000262178.6:c.836T>A ENSP00000262178.2:p.Val279Glu
ENST00000377633.7:c.788T>A ENSP00000366860.3:p.Val263Glu
ENST00000402066.5:c.1259T>A ENSP00000384497.1:p.Val420Glu
NM_001304522.1:c.596T>A NP_001291451.1:p.Val199Glu
NM_001308259.1:c.788T>A NP_001295188.1:p.Val263Glu
NM_003382.4:c.836T>A NP_003373.2:p.Val279Glu
NR_130758.1:n.1022T>A
XM_005249561.2:c.911T>A XP_005249618.1:p.Val304Glu
XM_006716107.1:c.836T>A XP_006716170.1:p.Val279Glu
XM_006716108.2:c.647T>A XP_006716171.1:p.Val216Glu
XM_011516550.1:c.788T>A XP_011514852.1:p.Val263Glu
XM_011516552.1:c.422T>A XP_011514854.1:p.Val141Glu
XR_242047.2:n.1231T>A
XM_005249561.3:c.911T>A XP_005249618.1:p.Val304Glu
XM_006716107.2:c.836T>A XP_006716170.1:p.Val279Glu
XM_006716108.3:c.647T>A XP_006716171.1:p.Val216Glu
XM_011516550.2:c.788T>A XP_011514852.1:p.Val263Glu
XM_017012580.1:c.422T>A XP_016868069.1:p.Val141Glu
XM_024446914.1:c.911T>A XP_024302682.1:p.Val304Glu
XM_024446915.1:c.911T>A XP_024302683.1:p.Val304Glu
XM_024446916.1:c.836T>A XP_024302684.1:p.Val279Glu
XM_024446917.1:c.647T>A XP_024302685.1:p.Val216Glu
XM_024446918.1:c.422T>A XP_024302686.1:p.Val141Glu
NM_003382.5:c.836T>A MANE Select NP_003373.2:p.Val279Glu
NM_001304522.2:c.596T>A NP_001291451.1:p.Val199Glu
NR_130758.2:n.932T>A