Canonical Allele Identifier: CA369941111
Gene: VIPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034586T>G , CM000669.2:g.159034586T>G GRCh38
NC_000007.13:g.158827277T>G , CM000669.1:g.158827277T>G GRCh37
NC_000007.12:g.158520038T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.874A>C MANE Select ENSP00000262178.2:p.Ile292Leu
ENST00000262178.6:c.874A>C ENSP00000262178.2:p.Ile292Leu
ENST00000377633.7:c.826A>C ENSP00000366860.3:p.Ile276Leu
ENST00000402066.5:c.1297A>C ENSP00000384497.1:p.Ile433Leu
NM_001304522.1:c.634A>C NP_001291451.1:p.Ile212Leu
NM_001308259.1:c.826A>C NP_001295188.1:p.Ile276Leu
NM_003382.4:c.874A>C NP_003373.2:p.Ile292Leu
NR_130758.1:n.1060A>C
XM_005249561.2:c.949A>C XP_005249618.1:p.Ile317Leu
XM_006716107.1:c.874A>C XP_006716170.1:p.Ile292Leu
XM_006716108.2:c.685A>C XP_006716171.1:p.Ile229Leu
XM_011516550.1:c.826A>C XP_011514852.1:p.Ile276Leu
XM_011516552.1:c.460A>C XP_011514854.1:p.Ile154Leu
XR_242047.2:n.1269A>C
XM_005249561.3:c.949A>C XP_005249618.1:p.Ile317Leu
XM_006716107.2:c.874A>C XP_006716170.1:p.Ile292Leu
XM_006716108.3:c.685A>C XP_006716171.1:p.Ile229Leu
XM_011516550.2:c.826A>C XP_011514852.1:p.Ile276Leu
XM_017012580.1:c.460A>C XP_016868069.1:p.Ile154Leu
XM_024446914.1:c.949A>C XP_024302682.1:p.Ile317Leu
XM_024446915.1:c.949A>C XP_024302683.1:p.Ile317Leu
XM_024446916.1:c.874A>C XP_024302684.1:p.Ile292Leu
XM_024446917.1:c.685A>C XP_024302685.1:p.Ile229Leu
XM_024446918.1:c.460A>C XP_024302686.1:p.Ile154Leu
NM_003382.5:c.874A>C MANE Select NP_003373.2:p.Ile292Leu
NM_001304522.2:c.634A>C NP_001291451.1:p.Ile212Leu
NR_130758.2:n.970A>C