Canonical Allele Identifier: CA369941654
Gene: VIPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034649A>C , CM000669.2:g.159034649A>C GRCh38
NC_000007.13:g.158827340A>C , CM000669.1:g.158827340A>C GRCh37
NC_000007.12:g.158520101A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.811T>G MANE Select ENSP00000262178.2:p.Cys271Gly
ENST00000262178.6:c.811T>G ENSP00000262178.2:p.Cys271Gly
ENST00000377633.7:c.763T>G ENSP00000366860.3:p.Cys255Gly
ENST00000402066.5:c.1234T>G ENSP00000384497.1:p.Cys412Gly
NM_001304522.1:c.571T>G NP_001291451.1:p.Cys191Gly
NM_001308259.1:c.763T>G NP_001295188.1:p.Cys255Gly
NM_003382.4:c.811T>G NP_003373.2:p.Cys271Gly
NR_130758.1:n.997T>G
XM_005249561.2:c.886T>G XP_005249618.1:p.Cys296Gly
XM_006716107.1:c.811T>G XP_006716170.1:p.Cys271Gly
XM_006716108.2:c.622T>G XP_006716171.1:p.Cys208Gly
XM_011516550.1:c.763T>G XP_011514852.1:p.Cys255Gly
XM_011516552.1:c.397T>G XP_011514854.1:p.Cys133Gly
XR_242047.2:n.1206T>G
XM_005249561.3:c.886T>G XP_005249618.1:p.Cys296Gly
XM_006716107.2:c.811T>G XP_006716170.1:p.Cys271Gly
XM_006716108.3:c.622T>G XP_006716171.1:p.Cys208Gly
XM_011516550.2:c.763T>G XP_011514852.1:p.Cys255Gly
XM_017012580.1:c.397T>G XP_016868069.1:p.Cys133Gly
XM_024446914.1:c.886T>G XP_024302682.1:p.Cys296Gly
XM_024446915.1:c.886T>G XP_024302683.1:p.Cys296Gly
XM_024446916.1:c.811T>G XP_024302684.1:p.Cys271Gly
XM_024446917.1:c.622T>G XP_024302685.1:p.Cys208Gly
XM_024446918.1:c.397T>G XP_024302686.1:p.Cys133Gly
NM_003382.5:c.811T>G MANE Select NP_003373.2:p.Cys271Gly
NM_001304522.2:c.571T>G NP_001291451.1:p.Cys191Gly
NR_130758.2:n.907T>G