Canonical Allele Identifier: CA1756436975
Gene: VIPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034677_159034679delinsTTA , CM000669.2:g.159034677_159034679delinsTTA GRCh38
NC_000007.13:g.158827368_158827370delinsTTA , CM000669.1:g.158827368_158827370delinsTTA GRCh37
NC_000007.12:g.158520129_158520131delinsTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.810-29_810-27delinsTAA MANE Select ENSP00000262178.2:n.810-29_810-27delinsTAA
ENST00000262178.6:c.810-29_810-27delinsTAA ENSP00000262178.2:n.810-29_810-27delinsTAA
ENST00000377633.7:c.762-29_762-27delinsTAA ENSP00000366860.3:n.762-29_762-27delinsTAA
ENST00000402066.5:c.1233-29_1233-27delinsTAA ENSP00000384497.1:n.1233-29_1233-27delinsTAA
NM_001304522.1:c.570-29_570-27delinsTAA NP_001291451.1:n.570-29_570-27delinsTAA
NM_001308259.1:c.762-29_762-27delinsTAA NP_001295188.1:n.762-29_762-27delinsTAA
NM_003382.4:c.810-29_810-27delinsTAA NP_003373.2:n.810-29_810-27delinsTAA
NR_130758.1:n.996-29_996-27delinsTAA
XM_005249561.2:c.885-29_885-27delinsTAA XP_005249618.1:n.885-29_885-27delinsTAA
XM_006716107.1:c.810-29_810-27delinsTAA XP_006716170.1:n.810-29_810-27delinsTAA
XM_006716108.2:c.621-29_621-27delinsTAA XP_006716171.1:n.621-29_621-27delinsTAA
XM_011516550.1:c.762-29_762-27delinsTAA XP_011514852.1:n.762-29_762-27delinsTAA
XM_011516552.1:c.396-29_396-27delinsTAA XP_011514854.1:n.396-29_396-27delinsTAA
XR_242047.2:n.1205-29_1205-27delinsTAA
XM_005249561.3:c.885-29_885-27delinsTAA XP_005249618.1:n.885-29_885-27delinsTAA
XM_006716107.2:c.810-29_810-27delinsTAA XP_006716170.1:n.810-29_810-27delinsTAA
XM_006716108.3:c.621-29_621-27delinsTAA XP_006716171.1:n.621-29_621-27delinsTAA
XM_011516550.2:c.762-29_762-27delinsTAA XP_011514852.1:n.762-29_762-27delinsTAA
XM_017012580.1:c.396-29_396-27delinsTAA XP_016868069.1:n.396-29_396-27delinsTAA
XM_024446914.1:c.885-29_885-27delinsTAA XP_024302682.1:n.885-29_885-27delinsTAA
XM_024446915.1:c.885-29_885-27delinsTAA XP_024302683.1:n.885-29_885-27delinsTAA
XM_024446916.1:c.810-29_810-27delinsTAA XP_024302684.1:n.810-29_810-27delinsTAA
XM_024446917.1:c.621-29_621-27delinsTAA XP_024302685.1:n.621-29_621-27delinsTAA
XM_024446918.1:c.396-29_396-27delinsTAA XP_024302686.1:n.396-29_396-27delinsTAA
NM_003382.5:c.810-29_810-27delinsTAA MANE Select NP_003373.2:n.810-29_810-27delinsTAA
NM_001304522.2:c.570-29_570-27delinsTAA NP_001291451.1:n.570-29_570-27delinsTAA
NR_130758.2:n.906-29_906-27delinsTAA